Canonical Allele Identifier: CA381125468

Gene: SLC22A12

Linked Data

• MyVariant Identifiers: chr11:g.64365999A>G (hg19) ; chr11:g.64598527A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598527A>G , CM000673.2:g.64598527A>G	GRCh38
NC_000011.9:g.64365999A>G , CM000673.1:g.64365999A>G	GRCh37
NC_000011.8:g.64122575A>G	NCBI36
NG_008110.1:g.12718A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377574.6:c.842A>G MANE Select	ENSP00000366797.1:p.Glu281Gly
ENST00000336464.7:c.740A>G	ENSP00000336836.7:p.Glu247Gly
ENST00000377567.6:c.518A>G	ENSP00000366790.2:p.Glu173Gly
ENST00000377572.5:c.518A>G	ENSP00000366795.1:p.Glu173Gly
ENST00000377574.5:c.842A>G	ENSP00000366797.1:p.Glu281Gly
ENST00000473690.5:c.179A>G	ENSP00000438437.1:p.Glu60Gly
NM_001276326.1:c.740A>G	NP_001263255.1:p.Glu247Gly
NM_001276327.1:c.518A>G	NP_001263256.1:p.Glu173Gly
NM_144585.3:c.842A>G	NP_653186.2:p.Glu281Gly
NM_153378.2:c.179A>G	NP_700357.1:p.Glu60Gly
XM_006718430.2:c.917A>G	XP_006718493.1:p.Glu306Gly
XM_006718431.2:c.812A>G	XP_006718494.1:p.Glu271Gly
XM_006718430.4:c.917A>G	XP_006718493.1:p.Glu306Gly
XM_006718431.4:c.812A>G	XP_006718494.1:p.Glu271Gly
NM_144585.4:c.842A>G MANE Select	NP_653186.2:p.Glu281Gly
NM_001276326.2:c.740A>G	NP_001263255.1:p.Glu247Gly
NM_153378.3:c.179A>G	NP_700357.1:p.Glu60Gly
NM_001276327.2:c.518A>G	NP_001263256.1:p.Glu173Gly