Canonical Allele Identifier: CA1978798786

Gene: SLC22A12

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598579G= , CM000673.2:g.64598579G=	GRCh38
NC_000011.9:g.64366051G= , CM000673.1:g.64366051G=	GRCh37
NC_000011.8:g.64122627G=	NCBI36
NG_008110.1:g.12770G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000377574.6:c.894G= MANE Select	ENSP00000366797.1:p.Glu298=
ENST00000336464.7:c.792G=	ENSP00000336836.7:p.Glu264=
ENST00000377567.6:c.570G=	ENSP00000366790.2:p.Glu190=
ENST00000377572.5:c.570G=	ENSP00000366795.1:p.Glu190=
ENST00000377574.5:c.894G=	ENSP00000366797.1:p.Glu298=
ENST00000473690.5:c.231G=	ENSP00000438437.1:p.Glu77=
NM_001276326.1:c.792G=	NP_001263255.1:p.Glu264=
NM_001276327.1:c.570G=	NP_001263256.1:p.Glu190=
NM_144585.3:c.894G=	NP_653186.2:p.Glu298=
NM_153378.2:c.231G=	NP_700357.1:p.Glu77=
XM_006718430.2:c.969G=	XP_006718493.1:p.Glu323=
XM_006718431.2:c.864G=	XP_006718494.1:p.Glu288=
XM_006718430.4:c.969G=	XP_006718493.1:p.Glu323=
XM_006718431.4:c.864G=	XP_006718494.1:p.Glu288=
NM_144585.4:c.894G= MANE Select	NP_653186.2:p.Glu298=
NM_001276326.2:c.792G=	NP_001263255.1:p.Glu264=
NM_153378.3:c.231G=	NP_700357.1:p.Glu77=
NM_001276327.2:c.570G=	NP_001263256.1:p.Glu190=