Canonical Allele Identifier: CA399788460

Gene: SLC4A1

Linked Data

• MyVariant Identifiers: chr17:g.42335787C>G (hg19) ; chr17:g.44258419C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44258419C>G , CM000679.2:g.44258419C>G	GRCh38
NC_000017.10:g.42335787C>G , CM000679.1:g.42335787C>G	GRCh37
NC_000017.9:g.39691313C>G	NCBI36
NG_007498.1:g.14716G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262418.12:c.1081G>C MANE Select	ENSP00000262418.6:p.Gly361Arg
ENST00000262418.10:c.1081G>C	ENSP00000262418.6:p.Gly361Arg
ENST00000399246.3:c.777+843G>C	ENSP00000382190.3:n.777+843G>C
ENST00000497360.5:n.1220G>C
NM_000342.3:c.1081G>C	NP_000333.1:p.Gly361Arg
XM_005257593.3:c.886G>C	XP_005257650.1:p.Gly296Arg
XM_011525129.1:c.1081G>C	XP_011523431.1:p.Gly361Arg
XM_011525130.1:c.1081G>C	XP_011523432.1:p.Gly361Arg
XM_011525131.1:c.1081G>C	XP_011523433.1:p.Gly361Arg
XM_005257593.5:c.886G>C	XP_005257650.1:p.Gly296Arg
XM_011525129.2:c.1081G>C	XP_011523431.1:p.Gly361Arg
NM_000342.4:c.1081G>C MANE Select	NP_000333.1:p.Gly361Arg