Canonical Allele Identifier: CA1677059181

Gene: SLC22A3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160436867_160436868delinsAT , CM000668.2:g.160436867_160436868delinsAT	GRCh38
NC_000006.11:g.160857899_160857900delinsAT , CM000668.1:g.160857899_160857900delinsAT	GRCh37
NC_000006.10:g.160777889_160777890delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1063_1064delinsAT MANE Select	ENSP00000275300.2:p.Met355=
ENST00000275300.2:c.1063_1064delinsAT	ENSP00000275300.2:p.Met355=
NM_021977.3:c.1063_1064delinsAT	NP_068812.1:p.Met355=
XM_005267106.3:c.670_671delinsAT	XP_005267163.1:p.Met224=
XM_011536075.1:c.607_608delinsAT	XP_011534377.1:p.Met203=
XM_011536076.1:c.607_608delinsAT	XP_011534378.1:p.Met203=
XM_011536077.1:c.607_608delinsAT	XP_011534379.1:p.Met203=
XR_245546.1:n.1018-5894_1018-5893delinsAT
XM_005267106.5:c.670_671delinsAT	XP_005267163.1:p.Met224=
XM_011536075.2:c.607_608delinsAT	XP_011534377.1:p.Met203=
XM_011536076.3:c.607_608delinsAT	XP_011534378.1:p.Met203=
XM_017011203.2:c.607_608delinsAT	XP_016866692.1:p.Met203=
XR_001743588.1:n.1018-130_1018-129delinsAT
XR_001743589.1:n.1018-5894_1018-5893delinsAT
NM_021977.4:c.1063_1064delinsAT MANE Select	NP_068812.1:p.Met355=