Canonical Allele Identifier: CA1978798724

Gene: SLC22A12

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598564T= , CM000673.2:g.64598564T=	GRCh38
NC_000011.9:g.64366036T= , CM000673.1:g.64366036T=	GRCh37
NC_000011.8:g.64122612T=	NCBI36
NG_008110.1:g.12755T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377574.6:c.879T= MANE Select	ENSP00000366797.1:p.Asp293=
ENST00000336464.7:c.777T=	ENSP00000336836.7:p.Asp259=
ENST00000377567.6:c.555T=	ENSP00000366790.2:p.Asp185=
ENST00000377572.5:c.555T=	ENSP00000366795.1:p.Asp185=
ENST00000377574.5:c.879T=	ENSP00000366797.1:p.Asp293=
ENST00000473690.5:c.216T=	ENSP00000438437.1:p.Asp72=
NM_001276326.1:c.777T=	NP_001263255.1:p.Asp259=
NM_001276327.1:c.555T=	NP_001263256.1:p.Asp185=
NM_144585.3:c.879T=	NP_653186.2:p.Asp293=
NM_153378.2:c.216T=	NP_700357.1:p.Asp72=
XM_006718430.2:c.954T=	XP_006718493.1:p.Asp318=
XM_006718431.2:c.849T=	XP_006718494.1:p.Asp283=
XM_006718430.4:c.954T=	XP_006718493.1:p.Asp318=
XM_006718431.4:c.849T=	XP_006718494.1:p.Asp283=
NM_144585.4:c.879T= MANE Select	NP_653186.2:p.Asp293=
NM_001276326.2:c.777T=	NP_001263255.1:p.Asp259=
NM_153378.3:c.216T=	NP_700357.1:p.Asp72=
NM_001276327.2:c.555T=	NP_001263256.1:p.Asp185=