Canonical Allele Identifier: CA1732759201

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701916C= , CM000669.2:g.107701916C=	GRCh38
NC_000007.13:g.107342361C= , CM000669.1:g.107342361C=	GRCh37
NC_000007.12:g.107129597C=	NCBI36
NG_008489.1:g.46282C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644269.2:c.1893C= MANE Select	ENSP00000494017.1:p.Thr631=
ENST00000644846.1:c.604C=
ENST00000265715.7:c.1893C=	ENSP00000265715.3:p.Thr631=
ENST00000492030.2:n.180C=
NM_000441.1:c.1893C=	NP_000432.1:p.Thr631=
XM_005250425.1:c.1893C=	XP_005250482.1:p.Thr631=
XM_005250425.2:c.1893C=	XP_005250482.1:p.Thr631=
XM_017012318.1:c.1815C=	XP_016867807.1:p.Thr605=
NM_000441.2:c.1893C= MANE Select	NP_000432.1:p.Thr631=