Canonical Allele Identifier: CA2838201304
Gene: OR2C3 HGNC NCBI
GCSAML HGNC NCBI
GCSAML-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.247529730_247529731delinsG , CM000663.2:g.247529730_247529731delinsG GRCh38
NC_000001.10:g.247693032_247693033delinsG , CM000663.1:g.247693032_247693033delinsG GRCh37
NC_000001.9:g.245759655_245759656delinsG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366487.4:c.*1818_*1819delinsC (OR2C3) ENSP00000355443.3:n.*1818_*1819delinsC
ENST00000641802.1:c.*1818_*1819delinsC (OR2C3) MANE Select ENSP00000493385.1:n.*1818_*1819delinsC
ENST00000673193.1:n.215+859_215+860delinsC (OR2C3)
ENST00000366489.5:c.-148+2676_-148+2677delinsG (GCSAML) ENSP00000355445.1:n.-148+2676_-148+2677delinsG
ENST00000366491.6:c.-264+2676_-264+2677delinsG (GCSAML) ENSP00000355447.2:n.-264+2676_-264+2677delinsG
ENST00000463359.5:c.-68+11122_-68+11123delinsG (GCSAML) ENSP00000434526.1:n.-68+11122_-68+11123delinsG
ENST00000526896.5:c.-57+2676_-57+2677delinsG (GCSAML) ENSP00000436079.1:n.-57+2676_-57+2677delinsG
ENST00000527084.5:c.-68+2676_-68+2677delinsG (GCSAML) ENSP00000432118.1:n.-68+2676_-68+2677delinsG
ENST00000527541.5:c.-8+2676_-8+2677delinsG (GCSAML) ENSP00000435110.1:n.-8+2676_-8+2677delinsG
ENST00000529512.5:c.-68+2676_-68+2677delinsG (GCSAML) ENSP00000434084.1:n.-68+2676_-68+2677delinsG
ENST00000531662.1:n.483+2676_483+2677delinsG (GCSAML)
ENST00000536561.5:c.-57+2676_-57+2677delinsG (GCSAML) ENSP00000446460.2:n.-57+2676_-57+2677delinsG
ENST00000623578.3:c.-68+2676_-68+2677delinsG (GCSAML) ENSP00000485175.1:n.-68+2676_-68+2677delinsG
NM_001281834.1:c.-264+2676_-264+2677delinsG (GCSAML) NP_001268763.1:n.-264+2676_-264+2677delinsG
NM_001281835.1:c.-148+2676_-148+2677delinsG (GCSAML) NP_001268764.1:n.-148+2676_-148+2677delinsG
NM_001281836.1:c.-68+2676_-68+2677delinsG (GCSAML) NP_001268765.1:n.-68+2676_-68+2677delinsG
NM_001281837.1:c.-68+2676_-68+2677delinsG (GCSAML) NP_001268766.1:n.-68+2676_-68+2677delinsG
NM_001281838.1:c.-8+2676_-8+2677delinsG (GCSAML) NP_001268767.1:n.-8+2676_-8+2677delinsG
NM_001281853.1:c.-57+2676_-57+2677delinsG (GCSAML) NP_001268782.1:n.-57+2676_-57+2677delinsG
NR_027309.2:n.215+859_215+860delinsC (GCSAML-AS1)
XM_011544098.1:c.143+2676_143+2677delinsG (GCSAML) XP_011542400.1:n.143+2676_143+2677delinsG
XM_011544099.1:c.-148+2676_-148+2677delinsG (GCSAML) XP_011542401.1:n.-148+2676_-148+2677delinsG
XM_011544100.1:c.99+2676_99+2677delinsG (GCSAML) XP_011542402.1:n.99+2676_99+2677delinsG
XM_024453417.1:c.-148+2676_-148+2677delinsG (GCSAML) XP_024309185.1:n.-148+2676_-148+2677delinsG
NM_001281834.2:c.-264+2676_-264+2677delinsG (GCSAML) NP_001268763.1:n.-264+2676_-264+2677delinsG
NM_001281835.2:c.-148+2676_-148+2677delinsG (GCSAML) NP_001268764.1:n.-148+2676_-148+2677delinsG
NM_001281836.2:c.-68+2676_-68+2677delinsG (GCSAML) NP_001268765.1:n.-68+2676_-68+2677delinsG
NM_001281838.2:c.-8+2676_-8+2677delinsG (GCSAML) NP_001268767.1:n.-8+2676_-8+2677delinsG
NM_198074.6:c.*1818_*1819delinsC (OR2C3) MANE Select NP_932340.4:n.*1818_*1819delinsC