Canonical Allele Identifier: CA2507323942

Gene: SLC4A2

Linked Data

• gnomAD v4: 7-151064461-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151064466dup , CM000669.2:g.151064466dup	GRCh38
NC_000007.13:g.150761553dup , CM000669.1:g.150761553dup	GRCh37
NC_000007.12:g.150392486dup	NCBI36
NG_051947.1:g.11267dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413384.7:c.218-60dup MANE Select	ENSP00000405600.2:n.218-60dup
ENST00000677246.1:c.218-60dup	ENSP00000504447.1:n.218-60dup
ENST00000310317.9:c.52-139dup	ENSP00000311402.5:n.52-139dup
ENST00000392826.6:c.191-60dup	ENSP00000376571.2:n.191-60dup
ENST00000413384.6:c.218-60dup	ENSP00000405600.2:n.218-60dup
ENST00000461735.1:c.176-60dup	ENSP00000419164.1:n.176-60dup
ENST00000463414.5:c.218-60dup	ENSP00000418584.1:n.218-60dup
ENST00000482950.5:c.218-60dup	ENSP00000419379.1:n.218-60dup
ENST00000483786.5:c.218-60dup	ENSP00000417808.1:n.218-60dup
ENST00000485713.5:c.218-60dup	ENSP00000419412.1:n.218-60dup
ENST00000490898.5:c.218-60dup	ENSP00000418114.1:n.218-60dup
ENST00000494125.1:n.551dup
NM_001199692.1:c.218-60dup	NP_001186621.1:n.218-60dup
NM_001199693.1:c.191-60dup	NP_001186622.1:n.191-60dup
NM_001199694.1:c.176-60dup	NP_001186623.1:n.176-60dup
NM_003040.3:c.218-60dup	NP_003031.3:n.218-60dup
XM_006716094.2:c.218-60dup	XP_006716157.1:n.218-60dup
XM_011516497.1:c.218-60dup	XP_011514799.1:n.218-60dup
NM_001199692.2:c.218-60dup	NP_001186621.1:n.218-60dup
NM_001199694.2:c.176-60dup	NP_001186623.1:n.176-60dup
XM_006716094.3:c.218-60dup	XP_006716157.1:n.218-60dup
NM_003040.4:c.218-60dup MANE Select	NP_003031.3:n.218-60dup
NM_001199692.3:c.218-60dup	NP_001186621.1:n.218-60dup