Canonical Allele Identifier: CA500285620

Gene: SLC4A1

Linked Data

• MyVariant Identifiers: chr17:g.42331959G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44254591G>C , CM000679.2:g.44254591G>C	GRCh38
NC_000017.10:g.42331959G>C , CM000679.1:g.42331959G>C	GRCh37
NC_000017.9:g.39687485G>C	NCBI36
NG_007498.1:g.18544C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262418.12:c.1962C>G MANE Select	ENSP00000262418.6:p.Gly654=
ENST00000262418.10:c.1962C>G	ENSP00000262418.6:p.Gly654=
ENST00000399246.3:c.864C>G	ENSP00000382190.3:p.Gly288=
NM_000342.3:c.1962C>G	NP_000333.1:p.Gly654=
XM_005257593.3:c.1767C>G	XP_005257650.1:p.Gly589=
XM_011525129.1:c.1872C>G	XP_011523431.1:p.Gly624=
XM_011525130.1:c.1962C>G	XP_011523432.1:p.Gly654=
XM_011525131.1:c.1962C>G	XP_011523433.1:p.Gly654=
XM_005257593.5:c.1767C>G	XP_005257650.1:p.Gly589=
XM_011525129.2:c.1872C>G	XP_011523431.1:p.Gly624=
NM_000342.4:c.1962C>G MANE Select	NP_000333.1:p.Gly654=