Canonical Allele Identifier: CA1978798806

Gene: SLC22A12

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598590T= , CM000673.2:g.64598590T=	GRCh38
NC_000011.9:g.64366062T= , CM000673.1:g.64366062T=	GRCh37
NC_000011.8:g.64122638T=	NCBI36
NG_008110.1:g.12781T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377574.6:c.905T= MANE Select	ENSP00000366797.1:p.Val302=
ENST00000336464.7:c.803T=	ENSP00000336836.7:p.Val268=
ENST00000377567.6:c.581T=	ENSP00000366790.2:p.Val194=
ENST00000377572.5:c.581T=	ENSP00000366795.1:p.Val194=
ENST00000377574.5:c.905T=	ENSP00000366797.1:p.Val302=
ENST00000473690.5:c.242T=	ENSP00000438437.1:p.Val81=
NM_001276326.1:c.803T=	NP_001263255.1:p.Val268=
NM_001276327.1:c.581T=	NP_001263256.1:p.Val194=
NM_144585.3:c.905T=	NP_653186.2:p.Val302=
NM_153378.2:c.242T=	NP_700357.1:p.Val81=
XM_006718430.2:c.980T=	XP_006718493.1:p.Val327=
XM_006718431.2:c.875T=	XP_006718494.1:p.Val292=
XM_006718430.4:c.980T=	XP_006718493.1:p.Val327=
XM_006718431.4:c.875T=	XP_006718494.1:p.Val292=
NM_144585.4:c.905T= MANE Select	NP_653186.2:p.Val302=
NM_001276326.2:c.803T=	NP_001263255.1:p.Val268=
NM_153378.3:c.242T=	NP_700357.1:p.Val81=
NM_001276327.2:c.581T=	NP_001263256.1:p.Val194=