Canonical Allele Identifier: CA821619960

Gene: SLC22A3

Linked Data

• dbSNP Id: rs1212675630
• gnomAD v3: 6-160436900-TTAAAAGC-T
• gnomAD v4: 6-160436900-TTAAAAGC-T
• MyVariant Identifiers: chr6:g.160857933_160857939del (hg19) ; chr6:g.160436901_160436907del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160436902_160436908del , CM000668.2:g.160436902_160436908del	GRCh38
NC_000006.11:g.160857934_160857940del , CM000668.1:g.160857934_160857940del	GRCh37
NC_000006.10:g.160777924_160777930del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1073+25_1073+31del MANE Select	ENSP00000275300.2:n.1073+25_1073+31del
ENST00000275300.2:c.1073+25_1073+31del	ENSP00000275300.2:n.1073+25_1073+31del
NM_021977.3:c.1073+25_1073+31del	NP_068812.1:n.1073+25_1073+31del
XM_005267106.3:c.680+25_680+31del	XP_005267163.1:n.680+25_680+31del
XM_011536075.1:c.617+25_617+31del	XP_011534377.1:n.617+25_617+31del
XM_011536076.1:c.617+25_617+31del	XP_011534378.1:n.617+25_617+31del
XM_011536077.1:c.617+25_617+31del	XP_011534379.1:n.617+25_617+31del
XR_245546.1:n.1018-5859_1018-5853del
XM_005267106.5:c.680+25_680+31del	XP_005267163.1:n.680+25_680+31del
XM_011536075.2:c.617+25_617+31del	XP_011534377.1:n.617+25_617+31del
XM_011536076.3:c.617+25_617+31del	XP_011534378.1:n.617+25_617+31del
XM_017011203.2:c.617+25_617+31del	XP_016866692.1:n.617+25_617+31del
XR_001743588.1:n.1018-95_1018-89del
XR_001743589.1:n.1018-5859_1018-5853del
NM_021977.4:c.1073+25_1073+31del MANE Select	NP_068812.1:n.1073+25_1073+31del