Canonical Allele Identifier: CA1732759239

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107701930T= , CM000669.2:g.107701930T=	GRCh38
NC_000007.13:g.107342375T= , CM000669.1:g.107342375T=	GRCh37
NC_000007.12:g.107129611T=	NCBI36
NG_008489.1:g.46296T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.1907T= MANE Select	ENSP00000494017.1:p.Ile636=
ENST00000644846.1:c.618T=
ENST00000265715.7:c.1907T=	ENSP00000265715.3:p.Ile636=
ENST00000492030.2:n.194T=
NM_000441.1:c.1907T=	NP_000432.1:p.Ile636=
XM_005250425.1:c.1907T=	XP_005250482.1:p.Ile636=
XM_005250425.2:c.1907T=	XP_005250482.1:p.Ile636=
XM_017012318.1:c.1829T=	XP_016867807.1:p.Ile610=
NM_000441.2:c.1907T= MANE Select	NP_000432.1:p.Ile636=