Canonical Allele Identifier: CA1677048034

Gene: SLC22A3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160387090_160387091delinsAG , CM000668.2:g.160387090_160387091delinsAG	GRCh38
NC_000006.11:g.160808122_160808123delinsAG , CM000668.1:g.160808122_160808123delinsAG	GRCh37
NC_000006.10:g.160728112_160728113delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.430-10889_430-10888delinsAG MANE Select	ENSP00000275300.2:n.430-10889_430-10888delinsAG
ENST00000275300.2:c.430-10889_430-10888delinsAG	ENSP00000275300.2:n.430-10889_430-10888delinsAG
NM_021977.3:c.430-10889_430-10888delinsAG	NP_068812.1:n.430-10889_430-10888delinsAG
XM_005267106.3:c.37-10889_37-10888delinsAG	XP_005267163.1:n.37-10889_37-10888delinsAG
XM_005267107.2:c.430-10889_430-10888delinsAG	XP_005267164.1:n.430-10889_430-10888delinsAG
XM_011536076.1:c.-27-10889_-27-10888delinsAG	XP_011534378.1:n.-27-10889_-27-10888delinsAG
XM_011536077.1:c.-27-10889_-27-10888delinsAG	XP_011534379.1:n.-27-10889_-27-10888delinsAG
XM_011536078.1:c.430-10889_430-10888delinsAG	XP_011534380.1:n.430-10889_430-10888delinsAG
XR_245546.1:n.472-10889_472-10888delinsAG
XR_943187.1:n.4906_4907delinsCT
XM_005267106.5:c.37-10889_37-10888delinsAG	XP_005267163.1:n.37-10889_37-10888delinsAG
XM_005267107.3:c.430-10889_430-10888delinsAG	XP_005267164.1:n.430-10889_430-10888delinsAG
XM_011536075.2:c.-5433_-5432delinsAG	XP_011534377.1:n.-5433_-5432delinsAG
XM_011536076.3:c.-27-10889_-27-10888delinsAG	XP_011534378.1:n.-27-10889_-27-10888delinsAG
XM_017011203.2:c.-27-10889_-27-10888delinsAG	XP_016866692.1:n.-27-10889_-27-10888delinsAG
XR_001743588.1:n.472-10889_472-10888delinsAG
XR_001743589.1:n.472-10889_472-10888delinsAG
NM_021977.4:c.430-10889_430-10888delinsAG MANE Select	NP_068812.1:n.430-10889_430-10888delinsAG