Canonical Allele Identifier: CA366345892

Gene: SLC22A3

Linked Data

• MyVariant Identifiers: chr6:g.160858093T>A (hg19) ; chr6:g.160437061T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160437061T>A , CM000668.2:g.160437061T>A	GRCh38
NC_000006.11:g.160858093T>A , CM000668.1:g.160858093T>A	GRCh37
NC_000006.10:g.160778083T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000275300.3:c.1138T>A MANE Select	ENSP00000275300.2:p.Tyr380Asn
ENST00000275300.2:c.1138T>A	ENSP00000275300.2:p.Tyr380Asn
NM_021977.3:c.1138T>A	NP_068812.1:p.Tyr380Asn
XM_005267106.3:c.745T>A	XP_005267163.1:p.Tyr249Asn
XM_011536075.1:c.682T>A	XP_011534377.1:p.Tyr228Asn
XM_011536076.1:c.682T>A	XP_011534378.1:p.Tyr228Asn
XM_011536077.1:c.682T>A	XP_011534379.1:p.Tyr228Asn
XR_245546.1:n.1018-5700T>A
XM_005267106.5:c.745T>A	XP_005267163.1:p.Tyr249Asn
XM_011536075.2:c.682T>A	XP_011534377.1:p.Tyr228Asn
XM_011536076.3:c.682T>A	XP_011534378.1:p.Tyr228Asn
XM_017011203.2:c.682T>A	XP_016866692.1:p.Tyr228Asn
XR_001743588.1:n.1082T>A
XR_001743589.1:n.1018-5700T>A
NM_021977.4:c.1138T>A MANE Select	NP_068812.1:p.Tyr380Asn