Canonical Allele Identifier: CA457093733

Gene: SLC26A4

Linked Data

• MyVariant Identifiers: chr7:g.107334922G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107694477G>A , CM000669.2:g.107694477G>A	GRCh38
NC_000007.13:g.107334922G>A , CM000669.1:g.107334922G>A	GRCh37
NC_000007.12:g.107122158G>A	NCBI36
NG_008489.1:g.38843G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1338G>A MANE Select	ENSP00000494017.1:p.Gln446=
ENST00000644846.1:c.49G>A
ENST00000265715.7:c.1338G>A	ENSP00000265715.3:p.Gln446=
ENST00000460748.1:n.441G>A
ENST00000477350.5:n.189-144G>A
ENST00000480841.5:n.187G>A
ENST00000497446.5:n.353G>A
NM_000441.1:c.1338G>A	NP_000432.1:p.Gln446=
XM_005250425.1:c.1338G>A	XP_005250482.1:p.Gln446=
XM_005250425.2:c.1338G>A	XP_005250482.1:p.Gln446=
XM_017012318.1:c.1264-144G>A	XP_016867807.1:n.1264-144G>A
NM_000441.2:c.1338G>A MANE Select	NP_000432.1:p.Gln446=