Canonical Allele Identifier: CA368842829

Gene: SLC26A4

Linked Data

• MyVariant Identifiers: chr7:g.107341553T>C (hg19) ; chr7:g.107701108T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701108T>C , CM000669.2:g.107701108T>C	GRCh38
NC_000007.13:g.107341553T>C , CM000669.1:g.107341553T>C	GRCh37
NC_000007.12:g.107128789T>C	NCBI36
NG_008489.1:g.45474T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1715T>C MANE Select	ENSP00000494017.1:p.Phe572Ser
ENST00000644846.1:c.426T>C
ENST00000265715.7:c.1715T>C	ENSP00000265715.3:p.Phe572Ser
ENST00000480841.5:n.564T>C
ENST00000492030.2:n.91-719T>C
NM_000441.1:c.1715T>C	NP_000432.1:p.Phe572Ser
XM_005250425.1:c.1715T>C	XP_005250482.1:p.Phe572Ser
XM_005250425.2:c.1715T>C	XP_005250482.1:p.Phe572Ser
XM_017012318.1:c.1637T>C	XP_016867807.1:p.Phe546Ser
NM_000441.2:c.1715T>C MANE Select	NP_000432.1:p.Phe572Ser