Canonical Allele Identifier: CA2346677441

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669063_3669065delinsCAG , CM000682.2:g.3669063_3669065delinsCAG	GRCh38
NC_000020.10:g.3649710_3649712delinsCAG , CM000682.1:g.3649710_3649712delinsCAG	GRCh37
NC_000020.9:g.3597710_3597712delinsCAG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2405-65_2405-63delinsCTG MANE Select	ENSP00000348912.3:n.2405-65_2405-63delins...
ENST00000350009.6:c.2327-65_2327-63delinsCTG	ENSP00000322550.5:n.2327-65_2327-63delins...
ENST00000356518.6:c.2405-65_2405-63delinsCTG	ENSP00000348912.2:n.2405-65_2405-63delins...
ENST00000379861.8:c.2405-68_2405-66delinsCTG	ENSP00000369190.4:n.2405-68_2405-66delins...
ENST00000466620.5:n.1966-65_1966-63delinsCTG
ENST00000483362.1:n.1328-65_1328-63delinsCTG
ENST00000617732.1:c.*1092-68_*1092-66delinsCTG	ENSP00000483343.1:n.*1092-68_*1092-66deli...
ENST00000619289.4:c.2045-68_2045-66delinsCTG	ENSP00000484600.1:n.2045-68_2045-66delins...
NM_001282447.1:c.2405-68_2405-66delinsCTG	NP_001269376.1:n.2405-68_2405-66delinsCTG...
NM_025220.3:c.2405-65_2405-63delinsCTG	NP_079496.1:n.2405-65_2405-63delinsCTG
NM_153202.2:c.2327-65_2327-63delinsCTG	NP_694882.1:n.2327-65_2327-63delinsCTG
XM_005260843.1:c.2444-65_2444-63delinsCTG	XP_005260900.1:n.2444-65_2444-63delinsCTG...
XM_006723639.1:c.2444-68_2444-66delinsCTG	XP_006723702.1:n.2444-68_2444-66delinsCTG...
XM_006723640.1:c.2435-65_2435-63delinsCTG	XP_006723703.1:n.2435-65_2435-63delinsCTG...
XM_011529366.1:c.2441-65_2441-63delinsCTG	XP_011527668.1:n.2441-65_2441-63delinsCTG...
XM_011529367.1:c.2402-65_2402-63delinsCTG	XP_011527669.1:n.2402-65_2402-63delinsCTG...
XM_011529368.1:c.2366-65_2366-63delinsCTG	XP_011527670.1:n.2366-65_2366-63delinsCTG...
XM_011529373.1:c.1442-65_1442-63delinsCTG	XP_011527675.1:n.1442-65_1442-63delinsCTG...
XR_937151.1:n.2456-65_2456-63delinsCTG
XR_937152.1:n.2456-68_2456-66delinsCTG
XR_937153.1:n.2429-68_2429-66delinsCTG
XR_937154.1:n.2429-68_2429-66delinsCTG
XR_937155.1:n.2350-68_2350-66delinsCTG
XR_937157.1:n.2352-68_2352-66delinsCTG
NM_001282447.2:c.2405-68_2405-66delinsCTG	NP_001269376.1:n.2405-68_2405-66delinsCTG...
NM_025220.4:c.2405-65_2405-63delinsCTG	NP_079496.1:n.2405-65_2405-63delinsCTG
NM_153202.3:c.2327-65_2327-63delinsCTG	NP_694882.1:n.2327-65_2327-63delinsCTG
XM_011529373.2:c.1442-65_1442-63delinsCTG	XP_011527675.1:n.1442-65_1442-63delinsCTG...
XR_001754405.1:n.2516-68_2516-66delinsCTG
XR_002958534.1:n.2625-68_2625-66delinsCTG
NM_001282447.3:c.2405-68_2405-66delinsCTG	NP_001269376.1:n.2405-68_2405-66delinsCTG...
NM_025220.5:c.2405-65_2405-63delinsCTG MANE Select	NP_079496.1:n.2405-65_2405-63delinsCTG
NM_153202.4:c.2327-65_2327-63delinsCTG	NP_694882.1:n.2327-65_2327-63delinsCTG