Canonical Allele Identifier: CA2346677666

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669530_3669531delinsCT , CM000682.2:g.3669530_3669531delinsCT	GRCh38
NC_000020.10:g.3650177_3650178delinsCT , CM000682.1:g.3650177_3650178delinsCT	GRCh37
NC_000020.9:g.3598177_3598178delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2332+15_2332+16delinsAG MANE Select	ENSP00000348912.3:n.2332+15_2332+16delinsAG
ENST00000350009.6:c.2254+15_2254+16delinsAG	ENSP00000322550.5:n.2254+15_2254+16delinsAG
ENST00000356518.6:c.2332+15_2332+16delinsAG	ENSP00000348912.2:n.2332+15_2332+16delinsAG
ENST00000379861.8:c.2332+15_2332+16delinsAG	ENSP00000369190.4:n.2332+15_2332+16delinsAG
ENST00000466620.5:n.1893+15_1893+16delinsAG
ENST00000483362.1:n.1095_1096delinsAG
ENST00000617732.1:c.*1019+15_*1019+16delinsAG	ENSP00000483343.1:n.*1019+15_*1019+16delinsAG
ENST00000619289.4:c.1972+15_1972+16delinsAG	ENSP00000484600.1:n.1972+15_1972+16delinsAG
NM_001282447.1:c.2332+15_2332+16delinsAG	NP_001269376.1:n.2332+15_2332+16delinsAG
NM_025220.3:c.2332+15_2332+16delinsAG	NP_079496.1:n.2332+15_2332+16delinsAG
NM_153202.2:c.2254+15_2254+16delinsAG	NP_694882.1:n.2254+15_2254+16delinsAG
XM_005260843.1:c.2371+15_2371+16delinsAG	XP_005260900.1:n.2371+15_2371+16delinsAG
XM_006723639.1:c.2371+15_2371+16delinsAG	XP_006723702.1:n.2371+15_2371+16delinsAG
XM_006723640.1:c.2362+15_2362+16delinsAG	XP_006723703.1:n.2362+15_2362+16delinsAG
XM_011529366.1:c.2368+15_2368+16delinsAG	XP_011527668.1:n.2368+15_2368+16delinsAG
XM_011529367.1:c.2329+15_2329+16delinsAG	XP_011527669.1:n.2329+15_2329+16delinsAG
XM_011529368.1:c.2293+15_2293+16delinsAG	XP_011527670.1:n.2293+15_2293+16delinsAG
XM_011529373.1:c.1369+15_1369+16delinsAG	XP_011527675.1:n.1369+15_1369+16delinsAG
XR_937151.1:n.2384-161_2384-160delinsAG
XR_937152.1:n.2384-161_2384-160delinsAG
XR_937153.1:n.2356+15_2356+16delinsAG
XR_937154.1:n.2356+15_2356+16delinsAG
XR_937155.1:n.2277+15_2277+16delinsAG
XR_937157.1:n.2279+15_2279+16delinsAG
NM_001282447.2:c.2332+15_2332+16delinsAG	NP_001269376.1:n.2332+15_2332+16delinsAG
NM_025220.4:c.2332+15_2332+16delinsAG	NP_079496.1:n.2332+15_2332+16delinsAG
NM_153202.3:c.2254+15_2254+16delinsAG	NP_694882.1:n.2254+15_2254+16delinsAG
XM_011529373.2:c.1369+15_1369+16delinsAG	XP_011527675.1:n.1369+15_1369+16delinsAG
XR_001754405.1:n.2443+15_2443+16delinsAG
XR_002958534.1:n.2552+15_2552+16delinsAG
NM_001282447.3:c.2332+15_2332+16delinsAG	NP_001269376.1:n.2332+15_2332+16delinsAG
NM_025220.5:c.2332+15_2332+16delinsAG MANE Select	NP_079496.1:n.2332+15_2332+16delinsAG
NM_153202.4:c.2254+15_2254+16delinsAG	NP_694882.1:n.2254+15_2254+16delinsAG