Canonical Allele Identifier: CA368847313
Gene: SLC26A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107715428G>A , CM000669.2:g.107715428G>A GRCh38
NC_000007.13:g.107355873G>A , CM000669.1:g.107355873G>A GRCh37
NC_000007.12:g.107143109G>A NCBI36
NG_008489.1:g.59794G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.2325G>A MANE Select ENSP00000494017.1:p.Met775Ile
ENST00000644846.1:c.981G>A
ENST00000265715.7:c.2325G>A ENSP00000265715.3:p.Met775Ile
ENST00000492030.2:n.511G>A
NM_000441.1:c.2325G>A NP_000432.1:p.Met775Ile
XM_005250425.1:c.2325G>A XP_005250482.1:p.Met775Ile
XM_005250425.2:c.2325G>A XP_005250482.1:p.Met775Ile
XM_017012318.1:c.2247G>A XP_016867807.1:p.Met749Ile
NM_000441.2:c.2325G>A MANE Select NP_000432.1:p.Met775Ile