Canonical Allele Identifier: CA381125557

Gene: SLC22A12

Linked Data

• MyVariant Identifiers: chr11:g.64366007C>G (hg19) ; chr11:g.64598535C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64598535C>G , CM000673.2:g.64598535C>G	GRCh38
NC_000011.9:g.64366007C>G , CM000673.1:g.64366007C>G	GRCh37
NC_000011.8:g.64122583C>G	NCBI36
NG_008110.1:g.12726C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377574.6:c.850C>G MANE Select	ENSP00000366797.1:p.Arg284Gly
ENST00000336464.7:c.748C>G	ENSP00000336836.7:p.Arg250Gly
ENST00000377567.6:c.526C>G	ENSP00000366790.2:p.Arg176Gly
ENST00000377572.5:c.526C>G	ENSP00000366795.1:p.Arg176Gly
ENST00000377574.5:c.850C>G	ENSP00000366797.1:p.Arg284Gly
ENST00000473690.5:c.187C>G	ENSP00000438437.1:p.Arg63Gly
NM_001276326.1:c.748C>G	NP_001263255.1:p.Arg250Gly
NM_001276327.1:c.526C>G	NP_001263256.1:p.Arg176Gly
NM_144585.3:c.850C>G	NP_653186.2:p.Arg284Gly
NM_153378.2:c.187C>G	NP_700357.1:p.Arg63Gly
XM_006718430.2:c.925C>G	XP_006718493.1:p.Arg309Gly
XM_006718431.2:c.820C>G	XP_006718494.1:p.Arg274Gly
XM_006718430.4:c.925C>G	XP_006718493.1:p.Arg309Gly
XM_006718431.4:c.820C>G	XP_006718494.1:p.Arg274Gly
NM_144585.4:c.850C>G MANE Select	NP_653186.2:p.Arg284Gly
NM_001276326.2:c.748C>G	NP_001263255.1:p.Arg250Gly
NM_153378.3:c.187C>G	NP_700357.1:p.Arg63Gly
NM_001276327.2:c.526C>G	NP_001263256.1:p.Arg176Gly