Canonical Allele Identifier: CA1978798602

Gene: SLC22A12

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598525A= , CM000673.2:g.64598525A=	GRCh38
NC_000011.9:g.64365997A= , CM000673.1:g.64365997A=	GRCh37
NC_000011.8:g.64122573A=	NCBI36
NG_008110.1:g.12716A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377574.6:c.840A= MANE Select	ENSP00000366797.1:p.Ala280=
ENST00000336464.7:c.738A=	ENSP00000336836.7:p.Ala246=
ENST00000377567.6:c.516A=	ENSP00000366790.2:p.Ala172=
ENST00000377572.5:c.516A=	ENSP00000366795.1:p.Ala172=
ENST00000377574.5:c.840A=	ENSP00000366797.1:p.Ala280=
ENST00000473690.5:c.177A=	ENSP00000438437.1:p.Ala59=
NM_001276326.1:c.738A=	NP_001263255.1:p.Ala246=
NM_001276327.1:c.516A=	NP_001263256.1:p.Ala172=
NM_144585.3:c.840A=	NP_653186.2:p.Ala280=
NM_153378.2:c.177A=	NP_700357.1:p.Ala59=
XM_006718430.2:c.915A=	XP_006718493.1:p.Ala305=
XM_006718431.2:c.810A=	XP_006718494.1:p.Ala270=
XM_006718430.4:c.915A=	XP_006718493.1:p.Ala305=
XM_006718431.4:c.810A=	XP_006718494.1:p.Ala270=
NM_144585.4:c.840A= MANE Select	NP_653186.2:p.Ala280=
NM_001276326.2:c.738A=	NP_001263255.1:p.Ala246=
NM_153378.3:c.177A=	NP_700357.1:p.Ala59=
NM_001276327.2:c.516A=	NP_001263256.1:p.Ala172=