Canonical Allele Identifier: CA1978798703

Gene: SLC22A12

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598555C= , CM000673.2:g.64598555C=	GRCh38
NC_000011.9:g.64366027C= , CM000673.1:g.64366027C=	GRCh37
NC_000011.8:g.64122603C=	NCBI36
NG_008110.1:g.12746C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377574.6:c.870C= MANE Select	ENSP00000366797.1:p.Gly290=
ENST00000336464.7:c.768C=	ENSP00000336836.7:p.Gly256=
ENST00000377567.6:c.546C=	ENSP00000366790.2:p.Gly182=
ENST00000377572.5:c.546C=	ENSP00000366795.1:p.Gly182=
ENST00000377574.5:c.870C=	ENSP00000366797.1:p.Gly290=
ENST00000473690.5:c.207C=	ENSP00000438437.1:p.Gly69=
NM_001276326.1:c.768C=	NP_001263255.1:p.Gly256=
NM_001276327.1:c.546C=	NP_001263256.1:p.Gly182=
NM_144585.3:c.870C=	NP_653186.2:p.Gly290=
NM_153378.2:c.207C=	NP_700357.1:p.Gly69=
XM_006718430.2:c.945C=	XP_006718493.1:p.Gly315=
XM_006718431.2:c.840C=	XP_006718494.1:p.Gly280=
XM_006718430.4:c.945C=	XP_006718493.1:p.Gly315=
XM_006718431.4:c.840C=	XP_006718494.1:p.Gly280=
NM_144585.4:c.870C= MANE Select	NP_653186.2:p.Gly290=
NM_001276326.2:c.768C=	NP_001263255.1:p.Gly256=
NM_153378.3:c.207C=	NP_700357.1:p.Gly69=
NM_001276327.2:c.546C=	NP_001263256.1:p.Gly182=