Canonical Allele Identifier: CA366345875

Gene: SLC22A3

Linked Data

• MyVariant Identifiers: chr6:g.160858085G>A (hg19) ; chr6:g.160437053G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160437053G>A , CM000668.2:g.160437053G>A	GRCh38
NC_000006.11:g.160858085G>A , CM000668.1:g.160858085G>A	GRCh37
NC_000006.10:g.160778075G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1130G>A MANE Select	ENSP00000275300.2:p.Gly377Asp
ENST00000275300.2:c.1130G>A	ENSP00000275300.2:p.Gly377Asp
NM_021977.3:c.1130G>A	NP_068812.1:p.Gly377Asp
XM_005267106.3:c.737G>A	XP_005267163.1:p.Gly246Asp
XM_011536075.1:c.674G>A	XP_011534377.1:p.Gly225Asp
XM_011536076.1:c.674G>A	XP_011534378.1:p.Gly225Asp
XM_011536077.1:c.674G>A	XP_011534379.1:p.Gly225Asp
XR_245546.1:n.1018-5708G>A
XM_005267106.5:c.737G>A	XP_005267163.1:p.Gly246Asp
XM_011536075.2:c.674G>A	XP_011534377.1:p.Gly225Asp
XM_011536076.3:c.674G>A	XP_011534378.1:p.Gly225Asp
XM_017011203.2:c.674G>A	XP_016866692.1:p.Gly225Asp
XR_001743588.1:n.1074G>A
XR_001743589.1:n.1018-5708G>A
NM_021977.4:c.1130G>A MANE Select	NP_068812.1:p.Gly377Asp