Canonical Allele Identifier: CA1978798734

Gene: SLC22A12

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598566G= , CM000673.2:g.64598566G=	GRCh38
NC_000011.9:g.64366038G= , CM000673.1:g.64366038G=	GRCh37
NC_000011.8:g.64122614G=	NCBI36
NG_008110.1:g.12757G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377574.6:c.881G= MANE Select	ENSP00000366797.1:p.Trp294=
ENST00000336464.7:c.779G=	ENSP00000336836.7:p.Trp260=
ENST00000377567.6:c.557G=	ENSP00000366790.2:p.Trp186=
ENST00000377572.5:c.557G=	ENSP00000366795.1:p.Trp186=
ENST00000377574.5:c.881G=	ENSP00000366797.1:p.Trp294=
ENST00000473690.5:c.218G=	ENSP00000438437.1:p.Trp73=
NM_001276326.1:c.779G=	NP_001263255.1:p.Trp260=
NM_001276327.1:c.557G=	NP_001263256.1:p.Trp186=
NM_144585.3:c.881G=	NP_653186.2:p.Trp294=
NM_153378.2:c.218G=	NP_700357.1:p.Trp73=
XM_006718430.2:c.956G=	XP_006718493.1:p.Trp319=
XM_006718431.2:c.851G=	XP_006718494.1:p.Trp284=
XM_006718430.4:c.956G=	XP_006718493.1:p.Trp319=
XM_006718431.4:c.851G=	XP_006718494.1:p.Trp284=
NM_144585.4:c.881G= MANE Select	NP_653186.2:p.Trp294=
NM_001276326.2:c.779G=	NP_001263255.1:p.Trp260=
NM_153378.3:c.218G=	NP_700357.1:p.Trp73=
NM_001276327.2:c.557G=	NP_001263256.1:p.Trp186=