Canonical Allele Identifier: CA1978798779

Gene: SLC22A12

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598576G= , CM000673.2:g.64598576G=	GRCh38
NC_000011.9:g.64366048G= , CM000673.1:g.64366048G=	GRCh37
NC_000011.8:g.64122624G=	NCBI36
NG_008110.1:g.12767G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377574.6:c.891G= MANE Select	ENSP00000366797.1:p.Gln297=
ENST00000336464.7:c.789G=	ENSP00000336836.7:p.Gln263=
ENST00000377567.6:c.567G=	ENSP00000366790.2:p.Gln189=
ENST00000377572.5:c.567G=	ENSP00000366795.1:p.Gln189=
ENST00000377574.5:c.891G=	ENSP00000366797.1:p.Gln297=
ENST00000473690.5:c.228G=	ENSP00000438437.1:p.Gln76=
NM_001276326.1:c.789G=	NP_001263255.1:p.Gln263=
NM_001276327.1:c.567G=	NP_001263256.1:p.Gln189=
NM_144585.3:c.891G=	NP_653186.2:p.Gln297=
NM_153378.2:c.228G=	NP_700357.1:p.Gln76=
XM_006718430.2:c.966G=	XP_006718493.1:p.Gln322=
XM_006718431.2:c.861G=	XP_006718494.1:p.Gln287=
XM_006718430.4:c.966G=	XP_006718493.1:p.Gln322=
XM_006718431.4:c.861G=	XP_006718494.1:p.Gln287=
NM_144585.4:c.891G= MANE Select	NP_653186.2:p.Gln297=
NM_001276326.2:c.789G=	NP_001263255.1:p.Gln263=
NM_153378.3:c.228G=	NP_700357.1:p.Gln76=
NM_001276327.2:c.567G=	NP_001263256.1:p.Gln189=