Canonical Allele Identifier: CA2346676931

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668078G= , CM000682.2:g.3668078G=	GRCh38
NC_000020.10:g.3648725G= , CM000682.1:g.3648725G=	GRCh37
NC_000020.9:g.3596725G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.*885C= MANE Select	ENSP00000348912.3:n.*885C=
ENST00000350009.6:c.*885C=	ENSP00000322550.5:n.*885C=
ENST00000356518.6:c.*885C=	ENSP00000348912.2:n.*885C=
ENST00000379861.8:c.*885C=	ENSP00000369190.4:n.*885C=
ENST00000466620.5:n.2888C=
ENST00000483362.1:n.2250C=
ENST00000619289.4:c.*885C=	ENSP00000484600.1:n.*885C=
NM_001282447.1:c.*885C=	NP_001269376.1:n.*885C=
NM_025220.3:c.*885C=	NP_079496.1:n.*885C=
NM_153202.2:c.*885C=	NP_694882.1:n.*885C=
XM_005260843.1:c.*885C=	XP_005260900.1:n.*885C=
XM_006723639.1:c.*885C=	XP_006723702.1:n.*885C=
XM_006723640.1:c.*885C=	XP_006723703.1:n.*885C=
XM_011529366.1:c.*885C=	XP_011527668.1:n.*885C=
XM_011529367.1:c.*885C=	XP_011527669.1:n.*885C=
XM_011529368.1:c.*885C=	XP_011527670.1:n.*885C=
XM_011529373.1:c.*885C=	XP_011527675.1:n.*885C=
XR_937153.1:n.3348C=
XR_937154.1:n.3348C=
XR_937155.1:n.3269C=
XR_937157.1:n.3271C=
NM_001282447.2:c.*885C=	NP_001269376.1:n.*885C=
NM_025220.4:c.*885C=	NP_079496.1:n.*885C=
NM_153202.3:c.*885C=	NP_694882.1:n.*885C=
XM_011529373.2:c.*885C=	XP_011527675.1:n.*885C=
XR_001754405.1:n.3435C=
XR_002958534.1:n.3544C=
NM_001282447.3:c.*885C=	NP_001269376.1:n.*885C=
NM_025220.5:c.*885C= MANE Select	NP_079496.1:n.*885C=
NM_153202.4:c.*885C=	NP_694882.1:n.*885C=