Canonical Allele Identifier: CA500618910

Gene: SLC4A1

Linked Data

• MyVariant Identifiers: chr17:g.42330703C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44253335C>T , CM000679.2:g.44253335C>T	GRCh38
NC_000017.10:g.42330703C>T , CM000679.1:g.42330703C>T	GRCh37
NC_000017.9:g.39686229C>T	NCBI36
NG_007498.1:g.19800G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000262418.12:c.2094G>A MANE Select	ENSP00000262418.6:p.Lys698=
ENST00000262418.10:c.2094G>A	ENSP00000262418.6:p.Lys698=
ENST00000399246.3:c.996G>A	ENSP00000382190.3:p.Lys332=
NM_000342.3:c.2094G>A	NP_000333.1:p.Lys698=
XM_005257593.3:c.1899G>A	XP_005257650.1:p.Lys633=
XM_011525129.1:c.2004G>A	XP_011523431.1:p.Lys668=
XM_011525130.1:c.2094G>A	XP_011523432.1:p.Lys698=
XM_005257593.5:c.1899G>A	XP_005257650.1:p.Lys633=
XM_011525129.2:c.2004G>A	XP_011523431.1:p.Lys668=
NM_000342.4:c.2094G>A MANE Select	NP_000333.1:p.Lys698=