Canonical Allele Identifier: CA1677059194

Gene: SLC22A3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160436900_160436907delinsTTAAAAGC , CM000668.2:g.160436900_160436907delinsTTAAAAGC	GRCh38
NC_000006.11:g.160857932_160857939delinsTTAAAAGC , CM000668.1:g.160857932_160857939delinsTTAAAAGC	GRCh37
NC_000006.10:g.160777922_160777929delinsTTAAAAGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1073+23_1073+30delinsTTAAAAGC MANE Select	ENSP00000275300.2:n.1073+23_1073+30delinsTTAAAAGC
ENST00000275300.2:c.1073+23_1073+30delinsTTAAAAGC	ENSP00000275300.2:n.1073+23_1073+30delinsTTAAAAGC
NM_021977.3:c.1073+23_1073+30delinsTTAAAAGC	NP_068812.1:n.1073+23_1073+30delinsTTAAAAGC
XM_005267106.3:c.680+23_680+30delinsTTAAAAGC	XP_005267163.1:n.680+23_680+30delinsTTAAAAGC
XM_011536075.1:c.617+23_617+30delinsTTAAAAGC	XP_011534377.1:n.617+23_617+30delinsTTAAAAGC
XM_011536076.1:c.617+23_617+30delinsTTAAAAGC	XP_011534378.1:n.617+23_617+30delinsTTAAAAGC
XM_011536077.1:c.617+23_617+30delinsTTAAAAGC	XP_011534379.1:n.617+23_617+30delinsTTAAAAGC
XR_245546.1:n.1018-5861_1018-5854delinsTTAAAAGC
XM_005267106.5:c.680+23_680+30delinsTTAAAAGC	XP_005267163.1:n.680+23_680+30delinsTTAAAAGC
XM_011536075.2:c.617+23_617+30delinsTTAAAAGC	XP_011534377.1:n.617+23_617+30delinsTTAAAAGC
XM_011536076.3:c.617+23_617+30delinsTTAAAAGC	XP_011534378.1:n.617+23_617+30delinsTTAAAAGC
XM_017011203.2:c.617+23_617+30delinsTTAAAAGC	XP_016866692.1:n.617+23_617+30delinsTTAAAAGC
XR_001743588.1:n.1018-97_1018-90delinsTTAAAAGC
XR_001743589.1:n.1018-5861_1018-5854delinsTTAAAAGC
NM_021977.4:c.1073+23_1073+30delinsTTAAAAGC MANE Select	NP_068812.1:n.1073+23_1073+30delinsTTAAAAGC