Canonical Allele Identifier: CA381126018

Gene: SLC22A12

Linked Data

• MyVariant Identifiers: chr11:g.64366059G>A (hg19) ; chr11:g.64598587G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598587G>A , CM000673.2:g.64598587G>A	GRCh38
NC_000011.9:g.64366059G>A , CM000673.1:g.64366059G>A	GRCh37
NC_000011.8:g.64122635G>A	NCBI36
NG_008110.1:g.12778G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377574.6:c.902G>A MANE Select	ENSP00000366797.1:p.Arg301Lys
ENST00000336464.7:c.800G>A	ENSP00000336836.7:p.Arg267Lys
ENST00000377567.6:c.578G>A	ENSP00000366790.2:p.Arg193Lys
ENST00000377572.5:c.578G>A	ENSP00000366795.1:p.Arg193Lys
ENST00000377574.5:c.902G>A	ENSP00000366797.1:p.Arg301Lys
ENST00000473690.5:c.239G>A	ENSP00000438437.1:p.Arg80Lys
NM_001276326.1:c.800G>A	NP_001263255.1:p.Arg267Lys
NM_001276327.1:c.578G>A	NP_001263256.1:p.Arg193Lys
NM_144585.3:c.902G>A	NP_653186.2:p.Arg301Lys
NM_153378.2:c.239G>A	NP_700357.1:p.Arg80Lys
XM_006718430.2:c.977G>A	XP_006718493.1:p.Arg326Lys
XM_006718431.2:c.872G>A	XP_006718494.1:p.Arg291Lys
XM_006718430.4:c.977G>A	XP_006718493.1:p.Arg326Lys
XM_006718431.4:c.872G>A	XP_006718494.1:p.Arg291Lys
NM_144585.4:c.902G>A MANE Select	NP_653186.2:p.Arg301Lys
NM_001276326.2:c.800G>A	NP_001263255.1:p.Arg267Lys
NM_153378.3:c.239G>A	NP_700357.1:p.Arg80Lys
NM_001276327.2:c.578G>A	NP_001263256.1:p.Arg193Lys