Canonical Allele Identifier: CA151207348

Gene: SLC22A3

Linked Data

• dbSNP Id: rs1008876207
• MyVariant Identifiers: chr6:g.160863506_160863513del (hg19) ; chr6:g.160442474_160442481del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160442480_160442487del , CM000668.2:g.160442480_160442487del	GRCh38
NC_000006.11:g.160863512_160863519del , CM000668.1:g.160863512_160863519del	GRCh37
NC_000006.10:g.160783502_160783509del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1289-281_1289-274del MANE Select	ENSP00000275300.2:n.1289-281_1289-274del
ENST00000275300.2:c.1289-281_1289-274del	ENSP00000275300.2:n.1289-281_1289-274del
NM_021977.3:c.1289-281_1289-274del	NP_068812.1:n.1289-281_1289-274del
XM_005267106.3:c.896-281_896-274del	XP_005267163.1:n.896-281_896-274del
XM_011536075.1:c.833-281_833-274del	XP_011534377.1:n.833-281_833-274del
XM_011536076.1:c.833-281_833-274del	XP_011534378.1:n.833-281_833-274del
XM_011536077.1:c.833-281_833-274del	XP_011534379.1:n.833-281_833-274del
XR_245546.1:n.1018-281_1018-274del
XM_005267106.5:c.896-281_896-274del	XP_005267163.1:n.896-281_896-274del
XM_011536075.2:c.833-281_833-274del	XP_011534377.1:n.833-281_833-274del
XM_011536076.3:c.833-281_833-274del	XP_011534378.1:n.833-281_833-274del
XM_017011203.2:c.833-281_833-274del	XP_016866692.1:n.833-281_833-274del
XR_001743588.1:n.1233-281_1233-274del
XR_001743589.1:n.1018-281_1018-274del
NM_021977.4:c.1289-281_1289-274del MANE Select	NP_068812.1:n.1289-281_1289-274del