Canonical Allele Identifier: CA1978798595

Gene: SLC22A12

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598519G= , CM000673.2:g.64598519G=	GRCh38
NC_000011.9:g.64365991G= , CM000673.1:g.64365991G=	GRCh37
NC_000011.8:g.64122567G=	NCBI36
NG_008110.1:g.12710G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377574.6:c.834G= MANE Select	ENSP00000366797.1:p.Trp278=
ENST00000336464.7:c.732G=	ENSP00000336836.7:p.Trp244=
ENST00000377567.6:c.510G=	ENSP00000366790.2:p.Trp170=
ENST00000377572.5:c.510G=	ENSP00000366795.1:p.Trp170=
ENST00000377574.5:c.834G=	ENSP00000366797.1:p.Trp278=
ENST00000473690.5:c.171G=	ENSP00000438437.1:p.Trp57=
NM_001276326.1:c.732G=	NP_001263255.1:p.Trp244=
NM_001276327.1:c.510G=	NP_001263256.1:p.Trp170=
NM_144585.3:c.834G=	NP_653186.2:p.Trp278=
NM_153378.2:c.171G=	NP_700357.1:p.Trp57=
XM_006718430.2:c.909G=	XP_006718493.1:p.Trp303=
XM_006718431.2:c.804G=	XP_006718494.1:p.Trp268=
XM_006718430.4:c.909G=	XP_006718493.1:p.Trp303=
XM_006718431.4:c.804G=	XP_006718494.1:p.Trp268=
NM_144585.4:c.834G= MANE Select	NP_653186.2:p.Trp278=
NM_001276326.2:c.732G=	NP_001263255.1:p.Trp244=
NM_153378.3:c.171G=	NP_700357.1:p.Trp57=
NM_001276327.2:c.510G=	NP_001263256.1:p.Trp170=