Canonical Allele Identifier: CA2651723650

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3669127-C-CTGGGCTGGGGAGGGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669127_3669128insTGGGCTGGGGAGGGAG , CM000682.2:g.3669127_3669128insTGGGCTGGGGAGGGAG	GRCh38
NC_000020.10:g.3649774_3649775insTGGGCTGGGGAGGGAG , CM000682.1:g.3649774_3649775insTGGGCTGGGGAGGGAG	GRCh37
NC_000020.9:g.3597774_3597775insTGGGCTGGGGAGGGAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2405-128_2405-127insCTCCCTCCCCAGCCCA MANE Select	ENSP00000348912.3:n.2405-128_2405-127insCTCCCTCCCCAGCCCA
ENST00000350009.6:c.2327-128_2327-127insCTCCCTCCCCAGCCCA	ENSP00000322550.5:n.2327-128_2327-127insCTCCCTCCCCAGCCCA
ENST00000356518.6:c.2405-128_2405-127insCTCCCTCCCCAGCCCA	ENSP00000348912.2:n.2405-128_2405-127insCTCCCTCCCCAGCCCA
ENST00000379861.8:c.2405-131_2405-130insCTCCCTCCCCAGCCCA	ENSP00000369190.4:n.2405-131_2405-130insCTCCCTCCCCAGCCCA
ENST00000466620.5:n.1966-128_1966-127insCTCCCTCCCCAGCCCA
ENST00000483362.1:n.1328-128_1328-127insCTCCCTCCCCAGCCCA
ENST00000617732.1:c.*1092-131_*1092-130insCTCCCTCCCCAGCCCA	ENSP00000483343.1:n.*1092-131_*1092-130insCTCCCTCCCCAGCCCA
ENST00000619289.4:c.2045-131_2045-130insCTCCCTCCCCAGCCCA	ENSP00000484600.1:n.2045-131_2045-130insCTCCCTCCCCAGCCCA
NM_001282447.1:c.2405-131_2405-130insCTCCCTCCCCAGCCCA	NP_001269376.1:n.2405-131_2405-130insCTCCCTCCCCAGCCCA
NM_025220.3:c.2405-128_2405-127insCTCCCTCCCCAGCCCA	NP_079496.1:n.2405-128_2405-127insCTCCCTCCCCAGCCCA
NM_153202.2:c.2327-128_2327-127insCTCCCTCCCCAGCCCA	NP_694882.1:n.2327-128_2327-127insCTCCCTCCCCAGCCCA
XM_005260843.1:c.2444-128_2444-127insCTCCCTCCCCAGCCCA	XP_005260900.1:n.2444-128_2444-127insCTCCCTCCCCAGCCCA
XM_006723639.1:c.2444-131_2444-130insCTCCCTCCCCAGCCCA	XP_006723702.1:n.2444-131_2444-130insCTCCCTCCCCAGCCCA
XM_006723640.1:c.2435-128_2435-127insCTCCCTCCCCAGCCCA	XP_006723703.1:n.2435-128_2435-127insCTCCCTCCCCAGCCCA
XM_011529366.1:c.2441-128_2441-127insCTCCCTCCCCAGCCCA	XP_011527668.1:n.2441-128_2441-127insCTCCCTCCCCAGCCCA
XM_011529367.1:c.2402-128_2402-127insCTCCCTCCCCAGCCCA	XP_011527669.1:n.2402-128_2402-127insCTCCCTCCCCAGCCCA
XM_011529368.1:c.2366-128_2366-127insCTCCCTCCCCAGCCCA	XP_011527670.1:n.2366-128_2366-127insCTCCCTCCCCAGCCCA
XM_011529373.1:c.1442-128_1442-127insCTCCCTCCCCAGCCCA	XP_011527675.1:n.1442-128_1442-127insCTCCCTCCCCAGCCCA
XR_937151.1:n.2456-128_2456-127insCTCCCTCCCCAGCCCA
XR_937152.1:n.2456-131_2456-130insCTCCCTCCCCAGCCCA
XR_937153.1:n.2429-131_2429-130insCTCCCTCCCCAGCCCA
XR_937154.1:n.2429-131_2429-130insCTCCCTCCCCAGCCCA
XR_937155.1:n.2350-131_2350-130insCTCCCTCCCCAGCCCA
XR_937157.1:n.2352-131_2352-130insCTCCCTCCCCAGCCCA
NM_001282447.2:c.2405-131_2405-130insCTCCCTCCCCAGCCCA	NP_001269376.1:n.2405-131_2405-130insCTCCCTCCCCAGCCCA
NM_025220.4:c.2405-128_2405-127insCTCCCTCCCCAGCCCA	NP_079496.1:n.2405-128_2405-127insCTCCCTCCCCAGCCCA
NM_153202.3:c.2327-128_2327-127insCTCCCTCCCCAGCCCA	NP_694882.1:n.2327-128_2327-127insCTCCCTCCCCAGCCCA
XM_011529373.2:c.1442-128_1442-127insCTCCCTCCCCAGCCCA	XP_011527675.1:n.1442-128_1442-127insCTCCCTCCCCAGCCCA
XR_001754405.1:n.2516-131_2516-130insCTCCCTCCCCAGCCCA
XR_002958534.1:n.2625-131_2625-130insCTCCCTCCCCAGCCCA
NM_001282447.3:c.2405-131_2405-130insCTCCCTCCCCAGCCCA	NP_001269376.1:n.2405-131_2405-130insCTCCCTCCCCAGCCCA
NM_025220.5:c.2405-128_2405-127insCTCCCTCCCCAGCCCA MANE Select	NP_079496.1:n.2405-128_2405-127insCTCCCTCCCCAGCCCA
NM_153202.4:c.2327-128_2327-127insCTCCCTCCCCAGCCCA	NP_694882.1:n.2327-128_2327-127insCTCCCTCCCCAGCCCA