Canonical Allele Identifier: CA399794398

Gene: SLC4A1

Linked Data

• MyVariant Identifiers: chr17:g.42337773T>G (hg19) ; chr17:g.44260405T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44260405T>G , CM000679.2:g.44260405T>G	GRCh38
NC_000017.10:g.42337773T>G , CM000679.1:g.42337773T>G	GRCh37
NC_000017.9:g.39693299T>G	NCBI36
NG_007498.1:g.12730A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262418.12:c.484A>C MANE Select	ENSP00000262418.6:p.Ser162Arg
ENST00000262418.10:c.484A>C	ENSP00000262418.6:p.Ser162Arg
ENST00000399246.3:c.484A>C	ENSP00000382190.3:p.Ser162Arg
ENST00000471005.5:n.418A>C
ENST00000497360.5:n.623A>C
NM_000342.3:c.484A>C	NP_000333.1:p.Ser162Arg
XM_005257593.3:c.289A>C	XP_005257650.1:p.Ser97Arg
XM_011525129.1:c.484A>C	XP_011523431.1:p.Ser162Arg
XM_011525130.1:c.484A>C	XP_011523432.1:p.Ser162Arg
XM_011525131.1:c.484A>C	XP_011523433.1:p.Ser162Arg
XM_005257593.5:c.289A>C	XP_005257650.1:p.Ser97Arg
XM_011525129.2:c.484A>C	XP_011523431.1:p.Ser162Arg
NM_000342.4:c.484A>C MANE Select	NP_000333.1:p.Ser162Arg