Canonical Allele Identifier: CA2346677715

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669608G= , CM000682.2:g.3669608G=	GRCh38
NC_000020.10:g.3650255G= , CM000682.1:g.3650255G=	GRCh37
NC_000020.9:g.3598255G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2270C= MANE Select	ENSP00000348912.3:p.Pro757=
ENST00000350009.6:c.2192C=	ENSP00000322550.5:p.Pro731=
ENST00000356518.6:c.2270C=	ENSP00000348912.2:p.Pro757=
ENST00000379861.8:c.2270C=	ENSP00000369190.4:p.Pro757=
ENST00000466620.5:n.1831C=
ENST00000483362.1:n.1018C=
ENST00000617732.1:c.*957C=	ENSP00000483343.1:n.*957C=
ENST00000619289.4:c.1910C=	ENSP00000484600.1:p.Pro637=
NM_001282447.1:c.2270C=	NP_001269376.1:p.Pro757=
NM_025220.3:c.2270C=	NP_079496.1:p.Pro757=
NM_153202.2:c.2192C=	NP_694882.1:p.Pro731=
XM_005260843.1:c.2309C=	XP_005260900.1:p.Pro770=
XM_006723639.1:c.2309C=	XP_006723702.1:p.Pro770=
XM_006723640.1:c.2300C=	XP_006723703.1:p.Pro767=
XM_011529366.1:c.2306C=	XP_011527668.1:p.Pro769=
XM_011529367.1:c.2267C=	XP_011527669.1:p.Pro756=
XM_011529368.1:c.2231C=	XP_011527670.1:p.Pro744=
XM_011529373.1:c.1307C=	XP_011527675.1:p.Pro436=
XR_937151.1:n.2384-238C=
XR_937152.1:n.2384-238C=
XR_937153.1:n.2294C=
XR_937154.1:n.2294C=
XR_937155.1:n.2215C=
XR_937157.1:n.2217C=
NM_001282447.2:c.2270C=	NP_001269376.1:p.Pro757=
NM_025220.4:c.2270C=	NP_079496.1:p.Pro757=
NM_153202.3:c.2192C=	NP_694882.1:p.Pro731=
XM_011529373.2:c.1307C=	XP_011527675.1:p.Pro436=
XR_001754405.1:n.2381C=
XR_002958534.1:n.2490C=
NM_001282447.3:c.2270C=	NP_001269376.1:p.Pro757=
NM_025220.5:c.2270C= MANE Select	NP_079496.1:p.Pro757=
NM_153202.4:c.2192C=	NP_694882.1:p.Pro731=