Canonical Allele Identifier: CA498430595
Gene: MYO15A HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.18049392T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18146078T>G , CM000679.2:g.18146078T>G GRCh38
NC_000017.10:g.18049392T>G , CM000679.1:g.18049392T>G GRCh37
NC_000017.9:g.17990117T>G NCBI36
NG_011634.1:g.42373T>G
NG_011634.2:g.42373T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647165.2:c.6480T>G MANE Select ENSP00000495481.1:p.Pro2160=
ENST00000205890.9:c.6480T>G ENSP00000205890.5:p.Pro2160=
ENST00000578999.1:n.65T>G
ENST00000615845.4:c.6480T>G ENSP00000481642.1:p.Pro2160=
NM_016239.3:c.6480T>G NP_057323.3:p.Pro2160=
XM_011523917.1:c.6420T>G XP_011522219.1:p.Pro2140=
XM_011523918.1:c.6342+78T>G XP_011522220.1:n.6342+78T>G
XM_011523921.1:c.6474T>G XP_011522223.1:p.Pro2158=
XR_934037.1:n.7079T>G
XR_934038.1:n.7079T>G
XM_011523918.2:c.6342+78T>G XP_011522220.1:n.6342+78T>G
XM_017024714.2:c.6420T>G XP_016880203.1:p.Pro2140=
XM_017024715.2:c.6483T>G XP_016880204.1:p.Pro2161=
XM_024450781.1:c.6213+1486T>G XP_024306549.1:n.6213+1486T>G
NM_016239.4:c.6480T>G MANE Select NP_057323.3:p.Pro2160=
Search 100 bp 5'
Search 100 bp 3'