Canonical Allele Identifier: CA1978798694

Gene: SLC22A12

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598549C= , CM000673.2:g.64598549C=	GRCh38
NC_000011.9:g.64366021C= , CM000673.1:g.64366021C=	GRCh37
NC_000011.8:g.64122597C=	NCBI36
NG_008110.1:g.12740C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377574.6:c.864C= MANE Select	ENSP00000366797.1:p.Thr288=
ENST00000336464.7:c.762C=	ENSP00000336836.7:p.Thr254=
ENST00000377567.6:c.540C=	ENSP00000366790.2:p.Thr180=
ENST00000377572.5:c.540C=	ENSP00000366795.1:p.Thr180=
ENST00000377574.5:c.864C=	ENSP00000366797.1:p.Thr288=
ENST00000473690.5:c.201C=	ENSP00000438437.1:p.Thr67=
NM_001276326.1:c.762C=	NP_001263255.1:p.Thr254=
NM_001276327.1:c.540C=	NP_001263256.1:p.Thr180=
NM_144585.3:c.864C=	NP_653186.2:p.Thr288=
NM_153378.2:c.201C=	NP_700357.1:p.Thr67=
XM_006718430.2:c.939C=	XP_006718493.1:p.Thr313=
XM_006718431.2:c.834C=	XP_006718494.1:p.Thr278=
XM_006718430.4:c.939C=	XP_006718493.1:p.Thr313=
XM_006718431.4:c.834C=	XP_006718494.1:p.Thr278=
NM_144585.4:c.864C= MANE Select	NP_653186.2:p.Thr288=
NM_001276326.2:c.762C=	NP_001263255.1:p.Thr254=
NM_153378.3:c.201C=	NP_700357.1:p.Thr67=
NM_001276327.2:c.540C=	NP_001263256.1:p.Thr180=