Canonical Allele Identifier: CA366345762

Gene: SLC22A3

Linked Data

• dbSNP Id: rs1788361382
• COSMIC: COSM41111
• MyVariant Identifiers: chr6:g.160858029G>T (hg19) ; chr6:g.160436997G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160436997G>T , CM000668.2:g.160436997G>T	GRCh38
NC_000006.11:g.160858029G>T , CM000668.1:g.160858029G>T	GRCh37
NC_000006.10:g.160778019G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1074G>T MANE Select	ENSP00000275300.2:p.Trp358Cys
ENST00000275300.2:c.1074G>T	ENSP00000275300.2:p.Trp358Cys
NM_021977.3:c.1074G>T	NP_068812.1:p.Trp358Cys
XM_005267106.3:c.681G>T	XP_005267163.1:p.Trp227Cys
XM_011536075.1:c.618G>T	XP_011534377.1:p.Trp206Cys
XM_011536076.1:c.618G>T	XP_011534378.1:p.Trp206Cys
XM_011536077.1:c.618G>T	XP_011534379.1:p.Trp206Cys
XR_245546.1:n.1018-5764G>T
XM_005267106.5:c.681G>T	XP_005267163.1:p.Trp227Cys
XM_011536075.2:c.618G>T	XP_011534377.1:p.Trp206Cys
XM_011536076.3:c.618G>T	XP_011534378.1:p.Trp206Cys
XM_017011203.2:c.618G>T	XP_016866692.1:p.Trp206Cys
XR_001743588.1:n.1018G>T
XR_001743589.1:n.1018-5764G>T
NM_021977.4:c.1074G>T MANE Select	NP_068812.1:p.Trp358Cys