Canonical Allele Identifier: CA2261306012

Gene: SLC4A1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44249667C= , CM000679.2:g.44249667C=	GRCh38
NC_000017.10:g.42327035C= , CM000679.1:g.42327035C=	GRCh37
NC_000017.9:g.39682561C=	NCBI36
NG_007498.1:g.23468G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.*791G= MANE Select	ENSP00000262418.6:n.*791G=
ENST00000262418.10:c.*791G=	ENSP00000262418.6:n.*791G=
ENST00000399246.3:c.*791G=	ENSP00000382190.3:n.*791G=
ENST00000631130.1:c.-417G=	ENSP00000486787.1:n.-417G=
NM_000342.3:c.*791G=	NP_000333.1:n.*791G=
XM_005257593.3:c.*791G=	XP_005257650.1:n.*791G=
XM_011525129.1:c.*791G=	XP_011523431.1:n.*791G=
XM_005257593.5:c.*791G=	XP_005257650.1:n.*791G=
XM_011525129.2:c.*791G=	XP_011523431.1:n.*791G=
NM_000342.4:c.*791G= MANE Select	NP_000333.1:n.*791G=