Canonical Allele Identifier: CA821623720

Gene: SLC22A3

Linked Data

• dbSNP Id: rs1477010639
• MyVariant Identifiers: chr6:g.160863422_160863455del (hg19) ; chr6:g.160442390_160442423del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160442393_160442426del , CM000668.2:g.160442393_160442426del	GRCh38
NC_000006.11:g.160863425_160863458del , CM000668.1:g.160863425_160863458del	GRCh37
NC_000006.10:g.160783415_160783448del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000275300.3:c.1289-368_1289-335del MANE Select	ENSP00000275300.2:n.1289-368_1289-335del
ENST00000275300.2:c.1289-368_1289-335del	ENSP00000275300.2:n.1289-368_1289-335del
NM_021977.3:c.1289-368_1289-335del	NP_068812.1:n.1289-368_1289-335del
XM_005267106.3:c.896-368_896-335del	XP_005267163.1:n.896-368_896-335del
XM_011536075.1:c.833-368_833-335del	XP_011534377.1:n.833-368_833-335del
XM_011536076.1:c.833-368_833-335del	XP_011534378.1:n.833-368_833-335del
XM_011536077.1:c.833-368_833-335del	XP_011534379.1:n.833-368_833-335del
XR_245546.1:n.1018-368_1018-335del
XM_005267106.5:c.896-368_896-335del	XP_005267163.1:n.896-368_896-335del
XM_011536075.2:c.833-368_833-335del	XP_011534377.1:n.833-368_833-335del
XM_011536076.3:c.833-368_833-335del	XP_011534378.1:n.833-368_833-335del
XM_017011203.2:c.833-368_833-335del	XP_016866692.1:n.833-368_833-335del
XR_001743588.1:n.1233-368_1233-335del
XR_001743589.1:n.1018-368_1018-335del
NM_021977.4:c.1289-368_1289-335del MANE Select	NP_068812.1:n.1289-368_1289-335del