Canonical Allele Identifier: CA1752501043

Gene: SLC4A2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151065784G>T , CM000669.2:g.151065784G>T	GRCh38
NC_000007.13:g.150762871G>T , CM000669.1:g.150762871G>T	GRCh37
NC_000007.12:g.150393804G>T	NCBI36
NG_051947.1:g.12585G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413384.7:c.579-733G>T MANE Select	ENSP00000405600.2:n.579-733G>T
ENST00000677246.1:c.579-733G>T	ENSP00000504447.1:n.579-733G>T
ENST00000310317.9:c.333-733G>T	ENSP00000311402.5:n.333-733G>T
ENST00000392826.6:c.552-733G>T	ENSP00000376571.2:n.552-733G>T
ENST00000413384.6:c.579-733G>T	ENSP00000405600.2:n.579-733G>T
ENST00000461735.1:c.537-733G>T	ENSP00000419164.1:n.537-733G>T
ENST00000485713.5:c.579-733G>T	ENSP00000419412.1:n.579-733G>T
NM_001199692.1:c.579-733G>T	NP_001186621.1:n.579-733G>T
NM_001199693.1:c.552-733G>T	NP_001186622.1:n.552-733G>T
NM_001199694.1:c.537-733G>T	NP_001186623.1:n.537-733G>T
NM_003040.3:c.579-733G>T	NP_003031.3:n.579-733G>T
XM_006716094.2:c.579-733G>T	XP_006716157.1:n.579-733G>T
XM_011516497.1:c.579-733G>T	XP_011514799.1:n.579-733G>T
NM_001199692.2:c.579-733G>T	NP_001186621.1:n.579-733G>T
NM_001199694.2:c.537-733G>T	NP_001186623.1:n.537-733G>T
XM_006716094.3:c.579-733G>T	XP_006716157.1:n.579-733G>T
NM_003040.4:c.579-733G>T MANE Select	NP_003031.3:n.579-733G>T
NM_001199692.3:c.579-733G>T	NP_001186621.1:n.579-733G>T