Canonical Allele Identifier: CA1677059263

Gene: SLC22A3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160437048_160437049delinsAG , CM000668.2:g.160437048_160437049delinsAG	GRCh38
NC_000006.11:g.160858080_160858081delinsAG , CM000668.1:g.160858080_160858081delinsAG	GRCh37
NC_000006.10:g.160778070_160778071delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1125_1126delinsAG MANE Select	ENSP00000275300.2:p.Ile375=
ENST00000275300.2:c.1125_1126delinsAG	ENSP00000275300.2:p.Ile375=
NM_021977.3:c.1125_1126delinsAG	NP_068812.1:p.Ile375=
XM_005267106.3:c.732_733delinsAG	XP_005267163.1:p.Ile244=
XM_011536075.1:c.669_670delinsAG	XP_011534377.1:p.Ile223=
XM_011536076.1:c.669_670delinsAG	XP_011534378.1:p.Ile223=
XM_011536077.1:c.669_670delinsAG	XP_011534379.1:p.Ile223=
XR_245546.1:n.1018-5713_1018-5712delinsAG
XM_005267106.5:c.732_733delinsAG	XP_005267163.1:p.Ile244=
XM_011536075.2:c.669_670delinsAG	XP_011534377.1:p.Ile223=
XM_011536076.3:c.669_670delinsAG	XP_011534378.1:p.Ile223=
XM_017011203.2:c.669_670delinsAG	XP_016866692.1:p.Ile223=
XR_001743588.1:n.1069_1070delinsAG
XR_001743589.1:n.1018-5713_1018-5712delinsAG
NM_021977.4:c.1125_1126delinsAG MANE Select	NP_068812.1:p.Ile375=