Canonical Allele Identifier: CA2528682175

Gene: SLC22A3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160386997_160386999del , CM000668.2:g.160386997_160386999del	GRCh38
NC_000006.11:g.160808029_160808031del , CM000668.1:g.160808029_160808031del	GRCh37
NC_000006.10:g.160728019_160728021del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.430-10982_430-10980del MANE Select	ENSP00000275300.2:n.430-10982_430-10980del
ENST00000275300.2:c.430-10982_430-10980del	ENSP00000275300.2:n.430-10982_430-10980del
NM_021977.3:c.430-10982_430-10980del	NP_068812.1:n.430-10982_430-10980del
XM_005267106.3:c.37-10982_37-10980del	XP_005267163.1:n.37-10982_37-10980del
XM_005267107.2:c.430-10982_430-10980del	XP_005267164.1:n.430-10982_430-10980del
XM_011536076.1:c.-27-10982_-27-10980del	XP_011534378.1:n.-27-10982_-27-10980del
XM_011536077.1:c.-27-10982_-27-10980del	XP_011534379.1:n.-27-10982_-27-10980del
XM_011536078.1:c.430-10982_430-10980del	XP_011534380.1:n.430-10982_430-10980del
XR_245546.1:n.472-10982_472-10980del
XR_943187.1:n.5004_5006del
XM_005267106.5:c.37-10982_37-10980del	XP_005267163.1:n.37-10982_37-10980del
XM_005267107.3:c.430-10982_430-10980del	XP_005267164.1:n.430-10982_430-10980del
XM_011536075.2:c.-5526_-5524del	XP_011534377.1:n.-5526_-5524del
XM_011536076.3:c.-27-10982_-27-10980del	XP_011534378.1:n.-27-10982_-27-10980del
XM_017011203.2:c.-27-10982_-27-10980del	XP_016866692.1:n.-27-10982_-27-10980del
XR_001743588.1:n.472-10982_472-10980del
XR_001743589.1:n.472-10982_472-10980del
NM_021977.4:c.430-10982_430-10980del MANE Select	NP_068812.1:n.430-10982_430-10980del