Canonical Allele Identifier: CA368840298

Gene: SLC26A4

Linked Data

• MyVariant Identifiers: chr7:g.107334878A>C (hg19) ; chr7:g.107694433A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107694433A>C , CM000669.2:g.107694433A>C	GRCh38
NC_000007.13:g.107334878A>C , CM000669.1:g.107334878A>C	GRCh37
NC_000007.12:g.107122114A>C	NCBI36
NG_008489.1:g.38799A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1294A>C MANE Select	ENSP00000494017.1:p.Met432Leu
ENST00000644846.1:c.5A>C
ENST00000265715.7:c.1294A>C	ENSP00000265715.3:p.Met432Leu
ENST00000460748.1:n.397A>C
ENST00000477350.5:n.189-188A>C
ENST00000480841.5:n.143A>C
ENST00000497446.5:n.309A>C
NM_000441.1:c.1294A>C	NP_000432.1:p.Met432Leu
XM_005250425.1:c.1294A>C	XP_005250482.1:p.Met432Leu
XM_005250425.2:c.1294A>C	XP_005250482.1:p.Met432Leu
XM_017012318.1:c.1264-188A>C	XP_016867807.1:n.1264-188A>C
NM_000441.2:c.1294A>C MANE Select	NP_000432.1:p.Met432Leu