Canonical Allele Identifier: CA2773798231

Gene: SLC22A3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160436835_160436843del , CM000668.2:g.160436835_160436843del	GRCh38
NC_000006.11:g.160857867_160857875del , CM000668.1:g.160857867_160857875del	GRCh37
NC_000006.10:g.160777857_160777865del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1031_1039del MANE Select	ENSP00000275300.2:p.Thr344_Gln346del
ENST00000275300.2:c.1031_1039del	ENSP00000275300.2:p.Thr344_Gln346del
NM_021977.3:c.1031_1039del	NP_068812.1:p.Thr344_Gln346del
XM_005267106.3:c.638_646del	XP_005267163.1:p.Thr213_Gln215del
XM_011536075.1:c.575_583del	XP_011534377.1:p.Thr192_Gln194del
XM_011536076.1:c.575_583del	XP_011534378.1:p.Thr192_Gln194del
XM_011536077.1:c.575_583del	XP_011534379.1:p.Thr192_Gln194del
XR_245546.1:n.1018-5926_1018-5918del
XM_005267106.5:c.638_646del	XP_005267163.1:p.Thr213_Gln215del
XM_011536075.2:c.575_583del	XP_011534377.1:p.Thr192_Gln194del
XM_011536076.3:c.575_583del	XP_011534378.1:p.Thr192_Gln194del
XM_017011203.2:c.575_583del	XP_016866692.1:p.Thr192_Gln194del
XR_001743588.1:n.1018-162_1018-154del
XR_001743589.1:n.1018-5926_1018-5918del
NM_021977.4:c.1031_1039del MANE Select	NP_068812.1:p.Thr344_Gln346del