Canonical Allele Identifier: CA1752479648

Gene: SLC4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151072139G= , CM000669.2:g.151072139G=	GRCh38
NC_000007.13:g.150769226G= , CM000669.1:g.150769226G=	GRCh37
NC_000007.12:g.150400159G=	NCBI36
NG_051947.1:g.18940G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413384.7:c.2535+3G= MANE Select	ENSP00000405600.2:n.2535+3G=
ENST00000677246.1:c.2535+3G=	ENSP00000504447.1:n.2535+3G=
ENST00000310317.9:c.2289+3G=	ENSP00000311402.5:n.2289+3G=
ENST00000392826.6:c.2508+3G=	ENSP00000376571.2:n.2508+3G=
ENST00000413384.6:c.2535+3G=	ENSP00000405600.2:n.2535+3G=
ENST00000460010.1:n.472+3G=
ENST00000461735.1:c.2493+3G=	ENSP00000419164.1:n.2493+3G=
ENST00000472204.1:n.133+3G=
ENST00000482697.1:n.304+3G=
ENST00000485713.5:c.2535+3G=	ENSP00000419412.1:n.2535+3G=
NM_001199692.1:c.2535+3G=	NP_001186621.1:n.2535+3G=
NM_001199693.1:c.2508+3G=	NP_001186622.1:n.2508+3G=
NM_001199694.1:c.2493+3G=	NP_001186623.1:n.2493+3G=
NM_003040.3:c.2535+3G=	NP_003031.3:n.2535+3G=
XM_011516497.1:c.2535+3G=	XP_011514799.1:n.2535+3G=
NM_001199692.2:c.2535+3G=	NP_001186621.1:n.2535+3G=
NM_001199694.2:c.2493+3G=	NP_001186623.1:n.2493+3G=
NM_003040.4:c.2535+3G= MANE Select	NP_003031.3:n.2535+3G=
NM_001199692.3:c.2535+3G=	NP_001186621.1:n.2535+3G=