Canonical Allele Identifier: CA457095841

Gene: SLC26A4

Linked Data

• gnomAD v4: 7-107695953-T-C
• MyVariant Identifiers: chr7:g.107336398T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107695953T>C , CM000669.2:g.107695953T>C	GRCh38
NC_000007.13:g.107336398T>C , CM000669.1:g.107336398T>C	GRCh37
NC_000007.12:g.107123634T>C	NCBI36
NG_008489.1:g.40319T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1458T>C MANE Select	ENSP00000494017.1:p.Cys486=
ENST00000644846.1:c.169T>C
ENST00000265715.7:c.1458T>C	ENSP00000265715.3:p.Cys486=
ENST00000460748.1:n.561T>C
ENST00000477350.5:n.305T>C
ENST00000480841.5:n.307T>C
ENST00000497446.5:n.473T>C
NM_000441.1:c.1458T>C	NP_000432.1:p.Cys486=
XM_005250425.1:c.1458T>C	XP_005250482.1:p.Cys486=
XM_005250425.2:c.1458T>C	XP_005250482.1:p.Cys486=
XM_017012318.1:c.1380T>C	XP_016867807.1:p.Cys460=
NM_000441.2:c.1458T>C MANE Select	NP_000432.1:p.Cys486=