Canonical Allele Identifier: CA2773796619

Gene: SLC22A3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160413753_160413758del , CM000668.2:g.160413753_160413758del	GRCh38
NC_000006.11:g.160834785_160834790del , CM000668.1:g.160834785_160834790del	GRCh37
NC_000006.10:g.160754775_160754780del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.975+2907_975+2912del MANE Select	ENSP00000275300.2:n.975+2907_975+2912del
ENST00000275300.2:c.975+2907_975+2912del	ENSP00000275300.2:n.975+2907_975+2912del
NM_021977.3:c.975+2907_975+2912del	NP_068812.1:n.975+2907_975+2912del
XM_005267106.3:c.582+2907_582+2912del	XP_005267163.1:n.582+2907_582+2912del
XM_005267107.2:c.975+2907_975+2912del	XP_005267164.1:n.975+2907_975+2912del
XM_011536075.1:c.519+2907_519+2912del	XP_011534377.1:n.519+2907_519+2912del
XM_011536076.1:c.519+2907_519+2912del	XP_011534378.1:n.519+2907_519+2912del
XM_011536077.1:c.519+2907_519+2912del	XP_011534379.1:n.519+2907_519+2912del
XM_011536078.1:c.975+2907_975+2912del	XP_011534380.1:n.975+2907_975+2912del
XR_245546.1:n.1017+2907_1017+2912del
XM_005267106.5:c.582+2907_582+2912del	XP_005267163.1:n.582+2907_582+2912del
XM_005267107.3:c.975+2907_975+2912del	XP_005267164.1:n.975+2907_975+2912del
XM_011536075.2:c.519+2907_519+2912del	XP_011534377.1:n.519+2907_519+2912del
XM_011536076.3:c.519+2907_519+2912del	XP_011534378.1:n.519+2907_519+2912del
XM_017011203.2:c.519+2907_519+2912del	XP_016866692.1:n.519+2907_519+2912del
XR_001743588.1:n.1017+2907_1017+2912del
XR_001743589.1:n.1017+2907_1017+2912del
NM_021977.4:c.975+2907_975+2912del MANE Select	NP_068812.1:n.975+2907_975+2912del