Canonical Allele Identifier: CA368840380

Gene: SLC26A4

Linked Data

• MyVariant Identifiers: chr7:g.107334900G>C (hg19) ; chr7:g.107694455G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107694455G>C , CM000669.2:g.107694455G>C	GRCh38
NC_000007.13:g.107334900G>C , CM000669.1:g.107334900G>C	GRCh37
NC_000007.12:g.107122136G>C	NCBI36
NG_008489.1:g.38821G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1316G>C MANE Select	ENSP00000494017.1:p.Gly439Ala
ENST00000644846.1:c.27G>C
ENST00000265715.7:c.1316G>C	ENSP00000265715.3:p.Gly439Ala
ENST00000460748.1:n.419G>C
ENST00000477350.5:n.189-166G>C
ENST00000480841.5:n.165G>C
ENST00000497446.5:n.331G>C
NM_000441.1:c.1316G>C	NP_000432.1:p.Gly439Ala
XM_005250425.1:c.1316G>C	XP_005250482.1:p.Gly439Ala
XM_005250425.2:c.1316G>C	XP_005250482.1:p.Gly439Ala
XM_017012318.1:c.1264-166G>C	XP_016867807.1:n.1264-166G>C
NM_000441.2:c.1316G>C MANE Select	NP_000432.1:p.Gly439Ala