Canonical Allele Identifier: CA1676973965

Gene: SLC22A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160247257T= , CM000668.2:g.160247257T=	GRCh38
NC_000006.11:g.160668289T= , CM000668.1:g.160668289T=	GRCh37
NC_000006.10:g.160588279T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366953.8:c.884A= MANE Select	ENSP00000355920.3:p.Lys295=
ENST00000366952.1:c.821A=	ENSP00000355919.1:p.Lys274=
ENST00000366953.7:c.884A=	ENSP00000355920.3:p.Lys295=
ENST00000491092.1:n.781A=
NM_003058.3:c.884A=	NP_003049.2:p.Lys295=
NM_003058.4:c.884A= MANE Select	NP_003049.2:p.Lys295=