Canonical Allele Identifier: CA399796402

Gene: SLC4A1

Linked Data

• MyVariant Identifiers: chr17:g.42338136C>G (hg19) ; chr17:g.44260768C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44260768C>G , CM000679.2:g.44260768C>G	GRCh38
NC_000017.10:g.42338136C>G , CM000679.1:g.42338136C>G	GRCh37
NC_000017.9:g.39693662C>G	NCBI36
NG_007498.1:g.12367G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.216G>C MANE Select	ENSP00000262418.6:p.Glu72Asp
ENST00000262418.10:c.216G>C	ENSP00000262418.6:p.Glu72Asp
ENST00000399246.3:c.216G>C	ENSP00000382190.3:p.Glu72Asp
ENST00000471005.5:n.150G>C
ENST00000497360.5:n.355G>C
NM_000342.3:c.216G>C	NP_000333.1:p.Glu72Asp
XM_005257593.3:c.21G>C	XP_005257650.1:p.Glu7Asp
XM_011525129.1:c.216G>C	XP_011523431.1:p.Glu72Asp
XM_011525130.1:c.216G>C	XP_011523432.1:p.Glu72Asp
XM_011525131.1:c.216G>C	XP_011523433.1:p.Glu72Asp
XM_005257593.5:c.21G>C	XP_005257650.1:p.Glu7Asp
XM_011525129.2:c.216G>C	XP_011523431.1:p.Glu72Asp
NM_000342.4:c.216G>C MANE Select	NP_000333.1:p.Glu72Asp