Canonical Allele Identifier: CA917904030

Gene: SLC22A3

Linked Data

• dbSNP Id: rs1583513043

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160437264_160437283del , CM000668.2:g.160437264_160437283del	GRCh38
NC_000006.11:g.160858296_160858315del , CM000668.1:g.160858296_160858315del	GRCh37
NC_000006.10:g.160778286_160778305del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1288+53_1288+72del MANE Select	ENSP00000275300.2:n.1288+53_1288+72del
ENST00000275300.2:c.1288+53_1288+72del	ENSP00000275300.2:n.1288+53_1288+72del
NM_021977.3:c.1288+53_1288+72del	NP_068812.1:n.1288+53_1288+72del
XM_005267106.3:c.895+53_895+72del	XP_005267163.1:n.895+53_895+72del
XM_011536075.1:c.832+53_832+72del	XP_011534377.1:n.832+53_832+72del
XM_011536076.1:c.832+53_832+72del	XP_011534378.1:n.832+53_832+72del
XM_011536077.1:c.832+53_832+72del	XP_011534379.1:n.832+53_832+72del
XR_245546.1:n.1018-5497_1018-5478del
XM_005267106.5:c.895+53_895+72del	XP_005267163.1:n.895+53_895+72del
XM_011536075.2:c.832+53_832+72del	XP_011534377.1:n.832+53_832+72del
XM_011536076.3:c.832+53_832+72del	XP_011534378.1:n.832+53_832+72del
XM_017011203.2:c.832+53_832+72del	XP_016866692.1:n.832+53_832+72del
XR_001743588.1:n.1232+53_1232+72del
XR_001743589.1:n.1018-5497_1018-5478del
NM_021977.4:c.1288+53_1288+72del MANE Select	NP_068812.1:n.1288+53_1288+72del