Canonical Allele Identifier: CA1677059411

Gene: SLC22A3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160437364_160437365delinsAC , CM000668.2:g.160437364_160437365delinsAC	GRCh38
NC_000006.11:g.160858396_160858397delinsAC , CM000668.1:g.160858396_160858397delinsAC	GRCh37
NC_000006.10:g.160778386_160778387delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1288+153_1288+154delinsAC MANE Select	ENSP00000275300.2:n.1288+153_1288+154delinsAC
ENST00000275300.2:c.1288+153_1288+154delinsAC	ENSP00000275300.2:n.1288+153_1288+154delinsAC
NM_021977.3:c.1288+153_1288+154delinsAC	NP_068812.1:n.1288+153_1288+154delinsAC
XM_005267106.3:c.895+153_895+154delinsAC	XP_005267163.1:n.895+153_895+154delinsAC
XM_011536075.1:c.832+153_832+154delinsAC	XP_011534377.1:n.832+153_832+154delinsAC
XM_011536076.1:c.832+153_832+154delinsAC	XP_011534378.1:n.832+153_832+154delinsAC
XM_011536077.1:c.832+153_832+154delinsAC	XP_011534379.1:n.832+153_832+154delinsAC
XR_245546.1:n.1018-5397_1018-5396delinsAC
XM_005267106.5:c.895+153_895+154delinsAC	XP_005267163.1:n.895+153_895+154delinsAC
XM_011536075.2:c.832+153_832+154delinsAC	XP_011534377.1:n.832+153_832+154delinsAC
XM_011536076.3:c.832+153_832+154delinsAC	XP_011534378.1:n.832+153_832+154delinsAC
XM_017011203.2:c.832+153_832+154delinsAC	XP_016866692.1:n.832+153_832+154delinsAC
XR_001743588.1:n.1232+153_1232+154delinsAC
XR_001743589.1:n.1018-5397_1018-5396delinsAC
NM_021977.4:c.1288+153_1288+154delinsAC MANE Select	NP_068812.1:n.1288+153_1288+154delinsAC