Canonical Allele Identifier: CA2832553422

Gene: SLC22A3

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1130dup MANE Select	ENSP00000275300.2:p.Asn378GlnfsTer25
ENST00000275300.2:c.1130dup	ENSP00000275300.2:p.Asn378GlnfsTer25
NM_021977.3:c.1130dup	NP_068812.1:p.Asn378GlnfsTer25
XM_005267106.3:c.737dup	XP_005267163.1:p.Asn247GlnfsTer25
XM_011536075.1:c.674dup	XP_011534377.1:p.Asn226GlnfsTer25
XM_011536076.1:c.674dup	XP_011534378.1:p.Asn226GlnfsTer25
XM_011536077.1:c.674dup	XP_011534379.1:p.Asn226GlnfsTer25
XR_245546.1:n.1018-5708dup
XM_005267106.5:c.737dup	XP_005267163.1:p.Asn247GlnfsTer25
XM_011536075.2:c.674dup	XP_011534377.1:p.Asn226GlnfsTer25
XM_011536076.3:c.674dup	XP_011534378.1:p.Asn226GlnfsTer25
XM_017011203.2:c.674dup	XP_016866692.1:p.Asn226GlnfsTer25
XR_001743588.1:n.1074dup
XR_001743589.1:n.1018-5708dup
NM_021977.4:c.1130dup MANE Select	NP_068812.1:p.Asn378GlnfsTer25