Canonical Allele Identifier: CA2346677567

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669304G= , CM000682.2:g.3669304G=	GRCh38
NC_000020.10:g.3649951G= , CM000682.1:g.3649951G=	GRCh37
NC_000020.9:g.3597951G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2399C= MANE Select	ENSP00000348912.3:p.Pro800=
ENST00000350009.6:c.2321C=	ENSP00000322550.5:p.Pro774=
ENST00000356518.6:c.2399C=	ENSP00000348912.2:p.Pro800=
ENST00000379861.8:c.2399C=	ENSP00000369190.4:p.Pro800=
ENST00000466620.5:n.1960C=
ENST00000483362.1:n.1322C=
ENST00000617732.1:c.*1086C=	ENSP00000483343.1:n.*1086C=
ENST00000619289.4:c.2039C=	ENSP00000484600.1:p.Pro680=
NM_001282447.1:c.2399C=	NP_001269376.1:p.Pro800=
NM_025220.3:c.2399C=	NP_079496.1:p.Pro800=
NM_153202.2:c.2321C=	NP_694882.1:p.Pro774=
XM_005260843.1:c.2438C=	XP_005260900.1:p.Pro813=
XM_006723639.1:c.2438C=	XP_006723702.1:p.Pro813=
XM_006723640.1:c.2429C=	XP_006723703.1:p.Pro810=
XM_011529366.1:c.2435C=	XP_011527668.1:p.Pro812=
XM_011529367.1:c.2396C=	XP_011527669.1:p.Pro799=
XM_011529368.1:c.2360C=	XP_011527670.1:p.Pro787=
XM_011529373.1:c.1436C=	XP_011527675.1:p.Pro479=
XR_937151.1:n.2450C=
XR_937152.1:n.2450C=
XR_937153.1:n.2423C=
XR_937154.1:n.2423C=
XR_937155.1:n.2344C=
XR_937157.1:n.2346C=
NM_001282447.2:c.2399C=	NP_001269376.1:p.Pro800=
NM_025220.4:c.2399C=	NP_079496.1:p.Pro800=
NM_153202.3:c.2321C=	NP_694882.1:p.Pro774=
XM_011529373.2:c.1436C=	XP_011527675.1:p.Pro479=
XR_001754405.1:n.2510C=
XR_002958534.1:n.2619C=
NM_001282447.3:c.2399C=	NP_001269376.1:p.Pro800=
NM_025220.5:c.2399C= MANE Select	NP_079496.1:p.Pro800=
NM_153202.4:c.2321C=	NP_694882.1:p.Pro774=