Canonical Allele Identifier: CA2261308252

Gene: SLC4A1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44254500T= , CM000679.2:g.44254500T=	GRCh38
NC_000017.10:g.42331868T= , CM000679.1:g.42331868T=	GRCh37
NC_000017.9:g.39687394T=	NCBI36
NG_007498.1:g.18635A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.2053A= MANE Select	ENSP00000262418.6:p.Thr685=
ENST00000262418.10:c.2053A=	ENSP00000262418.6:p.Thr685=
ENST00000399246.3:c.955A=	ENSP00000382190.3:p.Thr319=
NM_000342.3:c.2053A=	NP_000333.1:p.Thr685=
XM_005257593.3:c.1858A=	XP_005257650.1:p.Thr620=
XM_011525129.1:c.1963A=	XP_011523431.1:p.Thr655=
XM_011525130.1:c.2053A=	XP_011523432.1:p.Thr685=
XM_011525131.1:c.2053A=	XP_011523433.1:p.Thr685=
XM_005257593.5:c.1858A=	XP_005257650.1:p.Thr620=
XM_011525129.2:c.1963A=	XP_011523431.1:p.Thr655=
NM_000342.4:c.2053A= MANE Select	NP_000333.1:p.Thr685=