Canonical Allele Identifier: CA651093462

Gene: SLC22A3

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160442300_160442301insG , CM000668.2:g.160442300_160442301insG	GRCh38
NC_000006.11:g.160863332_160863333insG , CM000668.1:g.160863332_160863333insG	GRCh37
NC_000006.10:g.160783322_160783323insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1289-461_1289-460insG MANE Select	ENSP00000275300.2:n.1289-461_1289-460insG
ENST00000275300.2:c.1289-461_1289-460insG	ENSP00000275300.2:n.1289-461_1289-460insG
NM_021977.3:c.1289-461_1289-460insG	NP_068812.1:n.1289-461_1289-460insG
XM_005267106.3:c.896-461_896-460insG	XP_005267163.1:n.896-461_896-460insG
XM_011536075.1:c.833-461_833-460insG	XP_011534377.1:n.833-461_833-460insG
XM_011536076.1:c.833-461_833-460insG	XP_011534378.1:n.833-461_833-460insG
XM_011536077.1:c.833-461_833-460insG	XP_011534379.1:n.833-461_833-460insG
XR_245546.1:n.1018-461_1018-460insG
XM_005267106.5:c.896-461_896-460insG	XP_005267163.1:n.896-461_896-460insG
XM_011536075.2:c.833-461_833-460insG	XP_011534377.1:n.833-461_833-460insG
XM_011536076.3:c.833-461_833-460insG	XP_011534378.1:n.833-461_833-460insG
XM_017011203.2:c.833-461_833-460insG	XP_016866692.1:n.833-461_833-460insG
XR_001743588.1:n.1233-461_1233-460insG
XR_001743589.1:n.1018-461_1018-460insG
NM_021977.4:c.1289-461_1289-460insG MANE Select	NP_068812.1:n.1289-461_1289-460insG