Canonical Allele Identifier: CA4085122

Gene: SLC22A3

Linked Data

• dbSNP Id: rs770872659
• ExAC: 6:160857991 TCTTA / T
• gnomAD v2: 6-160857991-TCTTA-T
• gnomAD v3: 6-160436959-TCTTA-T
• gnomAD v4: 6-160436959-TCTTA-T
• MyVariant Identifiers: chr6:g.160857992_160857995del (hg19) ; chr6:g.160436960_160436963del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160436963_160436966del , CM000668.2:g.160436963_160436966del	GRCh38
NC_000006.11:g.160857995_160857998del , CM000668.1:g.160857995_160857998del	GRCh37
NC_000006.10:g.160777985_160777988del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1074-34_1074-31del MANE Select	ENSP00000275300.2:n.1074-34_1074-31del
ENST00000275300.2:c.1074-34_1074-31del	ENSP00000275300.2:n.1074-34_1074-31del
NM_021977.3:c.1074-34_1074-31del	NP_068812.1:n.1074-34_1074-31del
XM_005267106.3:c.681-34_681-31del	XP_005267163.1:n.681-34_681-31del
XM_011536075.1:c.618-34_618-31del	XP_011534377.1:n.618-34_618-31del
XM_011536076.1:c.618-34_618-31del	XP_011534378.1:n.618-34_618-31del
XM_011536077.1:c.618-34_618-31del	XP_011534379.1:n.618-34_618-31del
XR_245546.1:n.1018-5798_1018-5795del
XM_005267106.5:c.681-34_681-31del	XP_005267163.1:n.681-34_681-31del
XM_011536075.2:c.618-34_618-31del	XP_011534377.1:n.618-34_618-31del
XM_011536076.3:c.618-34_618-31del	XP_011534378.1:n.618-34_618-31del
XM_017011203.2:c.618-34_618-31del	XP_016866692.1:n.618-34_618-31del
XR_001743588.1:n.1018-34_1018-31del
XR_001743589.1:n.1018-5798_1018-5795del
NM_021977.4:c.1074-34_1074-31del MANE Select	NP_068812.1:n.1074-34_1074-31del