Canonical Allele Identifier: CA2346677459

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669079A= , CM000682.2:g.3669079A=	GRCh38
NC_000020.10:g.3649726A= , CM000682.1:g.3649726A=	GRCh37
NC_000020.9:g.3597726A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2405-79T= MANE Select	ENSP00000348912.3:n.2405-79T=
ENST00000350009.6:c.2327-79T=	ENSP00000322550.5:n.2327-79T=
ENST00000356518.6:c.2405-79T=	ENSP00000348912.2:n.2405-79T=
ENST00000379861.8:c.2405-82T=	ENSP00000369190.4:n.2405-82T=
ENST00000466620.5:n.1966-79T=
ENST00000483362.1:n.1328-79T=
ENST00000617732.1:c.*1092-82T=	ENSP00000483343.1:n.*1092-82T=
ENST00000619289.4:c.2045-82T=	ENSP00000484600.1:n.2045-82T=
NM_001282447.1:c.2405-82T=	NP_001269376.1:n.2405-82T=
NM_025220.3:c.2405-79T=	NP_079496.1:n.2405-79T=
NM_153202.2:c.2327-79T=	NP_694882.1:n.2327-79T=
XM_005260843.1:c.2444-79T=	XP_005260900.1:n.2444-79T=
XM_006723639.1:c.2444-82T=	XP_006723702.1:n.2444-82T=
XM_006723640.1:c.2435-79T=	XP_006723703.1:n.2435-79T=
XM_011529366.1:c.2441-79T=	XP_011527668.1:n.2441-79T=
XM_011529367.1:c.2402-79T=	XP_011527669.1:n.2402-79T=
XM_011529368.1:c.2366-79T=	XP_011527670.1:n.2366-79T=
XM_011529373.1:c.1442-79T=	XP_011527675.1:n.1442-79T=
XR_937151.1:n.2456-79T=
XR_937152.1:n.2456-82T=
XR_937153.1:n.2429-82T=
XR_937154.1:n.2429-82T=
XR_937155.1:n.2350-82T=
XR_937157.1:n.2352-82T=
NM_001282447.2:c.2405-82T=	NP_001269376.1:n.2405-82T=
NM_025220.4:c.2405-79T=	NP_079496.1:n.2405-79T=
NM_153202.3:c.2327-79T=	NP_694882.1:n.2327-79T=
XM_011529373.2:c.1442-79T=	XP_011527675.1:n.1442-79T=
XR_001754405.1:n.2516-82T=
XR_002958534.1:n.2625-82T=
NM_001282447.3:c.2405-82T=	NP_001269376.1:n.2405-82T=
NM_025220.5:c.2405-79T= MANE Select	NP_079496.1:n.2405-79T=
NM_153202.4:c.2327-79T=	NP_694882.1:n.2327-79T=