Canonical Allele Identifier: CA2261308072

Gene: SLC4A1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44254109A= , CM000679.2:g.44254109A=	GRCh38
NC_000017.10:g.42331477A= , CM000679.1:g.42331477A=	GRCh37
NC_000017.9:g.39687003A=	NCBI36
NG_007498.1:g.19026T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.2057+387T= MANE Select	ENSP00000262418.6:n.2057+387T=
ENST00000262418.10:c.2057+387T=	ENSP00000262418.6:n.2057+387T=
ENST00000399246.3:c.959+387T=	ENSP00000382190.3:n.959+387T=
NM_000342.3:c.2057+387T=	NP_000333.1:n.2057+387T=
XM_005257593.3:c.1862+387T=	XP_005257650.1:n.1862+387T=
XM_011525129.1:c.1967+387T=	XP_011523431.1:n.1967+387T=
XM_011525130.1:c.2057+387T=	XP_011523432.1:n.2057+387T=
XM_011525131.1:c.2058-301T=	XP_011523433.1:n.2058-301T=
XM_005257593.5:c.1862+387T=	XP_005257650.1:n.1862+387T=
XM_011525129.2:c.1967+387T=	XP_011523431.1:n.1967+387T=
NM_000342.4:c.2057+387T= MANE Select	NP_000333.1:n.2057+387T=