Canonical Allele Identifier: CA1978798708

Gene: SLC22A12

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598558G= , CM000673.2:g.64598558G=	GRCh38
NC_000011.9:g.64366030G= , CM000673.1:g.64366030G=	GRCh37
NC_000011.8:g.64122606G=	NCBI36
NG_008110.1:g.12749G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377574.6:c.873G= MANE Select	ENSP00000366797.1:p.Arg291=
ENST00000336464.7:c.771G=	ENSP00000336836.7:p.Arg257=
ENST00000377567.6:c.549G=	ENSP00000366790.2:p.Arg183=
ENST00000377572.5:c.549G=	ENSP00000366795.1:p.Arg183=
ENST00000377574.5:c.873G=	ENSP00000366797.1:p.Arg291=
ENST00000473690.5:c.210G=	ENSP00000438437.1:p.Arg70=
NM_001276326.1:c.771G=	NP_001263255.1:p.Arg257=
NM_001276327.1:c.549G=	NP_001263256.1:p.Arg183=
NM_144585.3:c.873G=	NP_653186.2:p.Arg291=
NM_153378.2:c.210G=	NP_700357.1:p.Arg70=
XM_006718430.2:c.948G=	XP_006718493.1:p.Arg316=
XM_006718431.2:c.843G=	XP_006718494.1:p.Arg281=
XM_006718430.4:c.948G=	XP_006718493.1:p.Arg316=
XM_006718431.4:c.843G=	XP_006718494.1:p.Arg281=
NM_144585.4:c.873G= MANE Select	NP_653186.2:p.Arg291=
NM_001276326.2:c.771G=	NP_001263255.1:p.Arg257=
NM_153378.3:c.210G=	NP_700357.1:p.Arg70=
NM_001276327.2:c.549G=	NP_001263256.1:p.Arg183=