Canonical Allele Identifier: CA1752500304

Gene: SLC4A2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151064230C= , CM000669.2:g.151064230C=	GRCh38
NC_000007.13:g.150761317C= , CM000669.1:g.150761317C=	GRCh37
NC_000007.12:g.150392250C=	NCBI36
NG_051947.1:g.11031C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413384.7:c.80C= MANE Select	ENSP00000405600.2:p.Thr27=
ENST00000677246.1:c.80C=	ENSP00000504447.1:p.Thr27=
ENST00000310317.9:c.52-375C=	ENSP00000311402.5:n.52-375C=
ENST00000392826.6:c.53C=	ENSP00000376571.2:p.Thr18=
ENST00000413384.6:c.80C=	ENSP00000405600.2:p.Thr27=
ENST00000461735.1:c.38C=	ENSP00000419164.1:p.Thr13=
ENST00000463414.5:c.80C=	ENSP00000418584.1:p.Thr27=
ENST00000482950.5:c.80C=	ENSP00000419379.1:p.Thr27=
ENST00000483786.5:c.80C=	ENSP00000417808.1:p.Thr27=
ENST00000485713.5:c.80C=	ENSP00000419412.1:p.Thr27=
ENST00000488420.1:c.80C=	ENSP00000417221.1:p.Thr27=
ENST00000490898.5:c.80C=	ENSP00000418114.1:p.Thr27=
ENST00000494125.1:n.315C=
NM_001199692.1:c.80C=	NP_001186621.1:p.Thr27=
NM_001199693.1:c.53C=	NP_001186622.1:p.Thr18=
NM_001199694.1:c.38C=	NP_001186623.1:p.Thr13=
NM_003040.3:c.80C=	NP_003031.3:p.Thr27=
XM_006716094.2:c.80C=	XP_006716157.1:p.Thr27=
XM_011516497.1:c.80C=	XP_011514799.1:p.Thr27=
NM_001199692.2:c.80C=	NP_001186621.1:p.Thr27=
NM_001199694.2:c.38C=	NP_001186623.1:p.Thr13=
XM_006716094.3:c.80C=	XP_006716157.1:p.Thr27=
NM_003040.4:c.80C= MANE Select	NP_003031.3:p.Thr27=
NM_001199692.3:c.80C=	NP_001186621.1:p.Thr27=