Canonical Allele Identifier: CA1732755874

Gene: SLC26A4

Linked Data

• dbSNP Id: rs1792339063

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107716092T>C , CM000669.2:g.107716092T>C	GRCh38
NC_000007.13:g.107356537T>C , CM000669.1:g.107356537T>C	GRCh37
NC_000007.12:g.107143773T>C	NCBI36
NG_008489.1:g.60458T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.*646T>C MANE Select	ENSP00000494017.1:n.*646T>C
ENST00000644846.1:c.1645T>C
ENST00000265715.7:c.*646T>C	ENSP00000265715.3:n.*646T>C
NM_000441.1:c.*646T>C	NP_000432.1:n.*646T>C
XM_005250425.2:c.*646T>C	XP_005250482.1:n.*646T>C
XM_017012318.1:c.*646T>C	XP_016867807.1:n.*646T>C
NM_000441.2:c.*646T>C MANE Select	NP_000432.1:n.*646T>C