Canonical Allele Identifier: CA821641173

Gene: SLC22A3

Linked Data

• dbSNP Id: rs1357071710
• gnomAD v3: 6-160386982-CAGG-C
• gnomAD v4: 6-160386982-CAGG-C
• MyVariant Identifiers: chr6:g.160808015_160808017del (hg19) ; chr6:g.160386983_160386985del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160386988_160386990del , CM000668.2:g.160386988_160386990del	GRCh38
NC_000006.11:g.160808020_160808022del , CM000668.1:g.160808020_160808022del	GRCh37
NC_000006.10:g.160728010_160728012del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.430-10991_430-10989del MANE Select	ENSP00000275300.2:n.430-10991_430-10989del
ENST00000275300.2:c.430-10991_430-10989del	ENSP00000275300.2:n.430-10991_430-10989del
NM_021977.3:c.430-10991_430-10989del	NP_068812.1:n.430-10991_430-10989del
XM_005267106.3:c.37-10991_37-10989del	XP_005267163.1:n.37-10991_37-10989del
XM_005267107.2:c.430-10991_430-10989del	XP_005267164.1:n.430-10991_430-10989del
XM_011536076.1:c.-27-10991_-27-10989del	XP_011534378.1:n.-27-10991_-27-10989del
XM_011536077.1:c.-27-10991_-27-10989del	XP_011534379.1:n.-27-10991_-27-10989del
XM_011536078.1:c.430-10991_430-10989del	XP_011534380.1:n.430-10991_430-10989del
XR_245546.1:n.472-10991_472-10989del
XR_943187.1:n.5012_5014del
XM_005267106.5:c.37-10991_37-10989del	XP_005267163.1:n.37-10991_37-10989del
XM_005267107.3:c.430-10991_430-10989del	XP_005267164.1:n.430-10991_430-10989del
XM_011536075.2:c.-5535_-5533del	XP_011534377.1:n.-5535_-5533del
XM_011536076.3:c.-27-10991_-27-10989del	XP_011534378.1:n.-27-10991_-27-10989del
XM_017011203.2:c.-27-10991_-27-10989del	XP_016866692.1:n.-27-10991_-27-10989del
XR_001743588.1:n.472-10991_472-10989del
XR_001743589.1:n.472-10991_472-10989del
NM_021977.4:c.430-10991_430-10989del MANE Select	NP_068812.1:n.430-10991_430-10989del