Canonical Allele Identifier: CA2651723676

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3669139-T-TGG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669139_3669140insGG , CM000682.2:g.3669139_3669140insGG	GRCh38
NC_000020.10:g.3649786_3649787insGG , CM000682.1:g.3649786_3649787insGG	GRCh37
NC_000020.9:g.3597786_3597787insGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2405-140_2405-139insCC MANE Select	ENSP00000348912.3:n.2405-140_2405-139insCC
ENST00000350009.6:c.2327-140_2327-139insCC	ENSP00000322550.5:n.2327-140_2327-139insCC
ENST00000356518.6:c.2405-140_2405-139insCC	ENSP00000348912.2:n.2405-140_2405-139insCC
ENST00000379861.8:c.2405-143_2405-142insCC	ENSP00000369190.4:n.2405-143_2405-142insCC
ENST00000466620.5:n.1966-140_1966-139insCC
ENST00000483362.1:n.1328-140_1328-139insCC
ENST00000617732.1:c.*1092-143_*1092-142insCC	ENSP00000483343.1:n.*1092-143_*1092-142insCC
ENST00000619289.4:c.2045-143_2045-142insCC	ENSP00000484600.1:n.2045-143_2045-142insCC
NM_001282447.1:c.2405-143_2405-142insCC	NP_001269376.1:n.2405-143_2405-142insCC
NM_025220.3:c.2405-140_2405-139insCC	NP_079496.1:n.2405-140_2405-139insCC
NM_153202.2:c.2327-140_2327-139insCC	NP_694882.1:n.2327-140_2327-139insCC
XM_005260843.1:c.2444-140_2444-139insCC	XP_005260900.1:n.2444-140_2444-139insCC
XM_006723639.1:c.2444-143_2444-142insCC	XP_006723702.1:n.2444-143_2444-142insCC
XM_006723640.1:c.2435-140_2435-139insCC	XP_006723703.1:n.2435-140_2435-139insCC
XM_011529366.1:c.2441-140_2441-139insCC	XP_011527668.1:n.2441-140_2441-139insCC
XM_011529367.1:c.2402-140_2402-139insCC	XP_011527669.1:n.2402-140_2402-139insCC
XM_011529368.1:c.2366-140_2366-139insCC	XP_011527670.1:n.2366-140_2366-139insCC
XM_011529373.1:c.1442-140_1442-139insCC	XP_011527675.1:n.1442-140_1442-139insCC
XR_937151.1:n.2456-140_2456-139insCC
XR_937152.1:n.2456-143_2456-142insCC
XR_937153.1:n.2429-143_2429-142insCC
XR_937154.1:n.2429-143_2429-142insCC
XR_937155.1:n.2350-143_2350-142insCC
XR_937157.1:n.2352-143_2352-142insCC
NM_001282447.2:c.2405-143_2405-142insCC	NP_001269376.1:n.2405-143_2405-142insCC
NM_025220.4:c.2405-140_2405-139insCC	NP_079496.1:n.2405-140_2405-139insCC
NM_153202.3:c.2327-140_2327-139insCC	NP_694882.1:n.2327-140_2327-139insCC
XM_011529373.2:c.1442-140_1442-139insCC	XP_011527675.1:n.1442-140_1442-139insCC
XR_001754405.1:n.2516-143_2516-142insCC
XR_002958534.1:n.2625-143_2625-142insCC
NM_001282447.3:c.2405-143_2405-142insCC	NP_001269376.1:n.2405-143_2405-142insCC
NM_025220.5:c.2405-140_2405-139insCC MANE Select	NP_079496.1:n.2405-140_2405-139insCC
NM_153202.4:c.2327-140_2327-139insCC	NP_694882.1:n.2327-140_2327-139insCC