Canonical Allele Identifier: CA1732747511
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1791506734

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107689338del , CM000669.2:g.107689338del GRCh38
NC_000007.13:g.107329783del , CM000669.1:g.107329783del GRCh37
NC_000007.12:g.107117019del NCBI36
NG_008489.1:g.33704del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1149+138del MANE Select ENSP00000494017.1:n.1149+138del
ENST00000265715.7:c.1149+138del ENSP00000265715.3:n.1149+138del
NM_000441.1:c.1149+138del NP_000432.1:n.1149+138del
XM_005250425.1:c.1149+138del XP_005250482.1:n.1149+138del
XM_006716025.2:c.1149+138del XP_006716088.1:n.1149+138del
XM_005250425.2:c.1149+138del XP_005250482.1:n.1149+138del
XM_006716025.3:c.1149+138del XP_006716088.1:n.1149+138del
XM_017012318.1:c.1149+138del XP_016867807.1:n.1149+138del
NM_000441.2:c.1149+138del MANE Select NP_000432.1:n.1149+138del