Canonical Allele Identifier: CA2685635030

Gene: SLC4A2

Linked Data

• gnomAD v4: 7-151064066-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151064066A>C , CM000669.2:g.151064066A>C	GRCh38
NC_000007.13:g.150761153A>C , CM000669.1:g.150761153A>C	GRCh37
NC_000007.12:g.150392086A>C	NCBI36
NG_051947.1:g.10867A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413384.7:c.52-136A>C MANE Select	ENSP00000405600.2:n.52-136A>C
ENST00000677246.1:c.52-136A>C	ENSP00000504447.1:n.52-136A>C
ENST00000310317.9:c.52-539A>C	ENSP00000311402.5:n.52-539A>C
ENST00000392826.6:c.25-136A>C	ENSP00000376571.2:n.25-136A>C
ENST00000413384.6:c.52-136A>C	ENSP00000405600.2:n.52-136A>C
ENST00000461735.1:c.10-136A>C	ENSP00000419164.1:n.10-136A>C
ENST00000463414.5:c.52-136A>C	ENSP00000418584.1:n.52-136A>C
ENST00000482950.5:c.52-136A>C	ENSP00000419379.1:n.52-136A>C
ENST00000483786.5:c.52-136A>C	ENSP00000417808.1:n.52-136A>C
ENST00000485713.5:c.52-136A>C	ENSP00000419412.1:n.52-136A>C
ENST00000488420.1:c.52-136A>C	ENSP00000417221.1:n.52-136A>C
ENST00000490898.5:c.52-136A>C	ENSP00000418114.1:n.52-136A>C
ENST00000494125.1:n.287-136A>C
NM_001199692.1:c.52-136A>C	NP_001186621.1:n.52-136A>C
NM_001199693.1:c.25-136A>C	NP_001186622.1:n.25-136A>C
NM_001199694.1:c.10-136A>C	NP_001186623.1:n.10-136A>C
NM_003040.3:c.52-136A>C	NP_003031.3:n.52-136A>C
XM_006716094.2:c.52-136A>C	XP_006716157.1:n.52-136A>C
XM_011516497.1:c.52-136A>C	XP_011514799.1:n.52-136A>C
NM_001199692.2:c.52-136A>C	NP_001186621.1:n.52-136A>C
NM_001199694.2:c.10-136A>C	NP_001186623.1:n.10-136A>C
XM_006716094.3:c.52-136A>C	XP_006716157.1:n.52-136A>C
NM_003040.4:c.52-136A>C MANE Select	NP_003031.3:n.52-136A>C
NM_001199692.3:c.52-136A>C	NP_001186621.1:n.52-136A>C