Canonical Allele Identifier: CA457093496

Gene: SLC26A4

Linked Data

• MyVariant Identifiers: chr7:g.107334877G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107694432G>T , CM000669.2:g.107694432G>T	GRCh38
NC_000007.13:g.107334877G>T , CM000669.1:g.107334877G>T	GRCh37
NC_000007.12:g.107122113G>T	NCBI36
NG_008489.1:g.38798G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1293G>T MANE Select	ENSP00000494017.1:p.Val431=
ENST00000644846.1:c.4G>T
ENST00000265715.7:c.1293G>T	ENSP00000265715.3:p.Val431=
ENST00000460748.1:n.396G>T
ENST00000477350.5:n.189-189G>T
ENST00000480841.5:n.142G>T
ENST00000497446.5:n.308G>T
NM_000441.1:c.1293G>T	NP_000432.1:p.Val431=
XM_005250425.1:c.1293G>T	XP_005250482.1:p.Val431=
XM_005250425.2:c.1293G>T	XP_005250482.1:p.Val431=
XM_017012318.1:c.1264-189G>T	XP_016867807.1:n.1264-189G>T
NM_000441.2:c.1293G>T MANE Select	NP_000432.1:p.Val431=