Canonical Allele Identifier: CA1732736038

Gene: SLC26A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107663366C= , CM000669.2:g.107663366C=	GRCh38
NC_000007.13:g.107303811C= , CM000669.1:g.107303811C=	GRCh37
NC_000007.12:g.107091047C=	NCBI36
NG_008489.1:g.7732C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644269.2:c.235C= MANE Select	ENSP00000494017.1:p.Arg79=
ENST00000265715.7:c.235C=	ENSP00000265715.3:p.Arg79=
ENST00000440056.1:c.235C=	ENSP00000394760.1:p.Arg79=
NM_000441.1:c.235C=	NP_000432.1:p.Arg79=
XM_005250425.1:c.235C=	XP_005250482.1:p.Arg79=
XM_006716025.2:c.235C=	XP_006716088.1:p.Arg79=
XM_005250425.2:c.235C=	XP_005250482.1:p.Arg79=
XM_006716025.3:c.235C=	XP_006716088.1:p.Arg79=
XM_017012318.1:c.235C=	XP_016867807.1:p.Arg79=
NM_000441.2:c.235C= MANE Select	NP_000432.1:p.Arg79=