Canonical Allele Identifier: CA2346677383

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668972G= , CM000682.2:g.3668972G=	GRCh38
NC_000020.10:g.3649619G= , CM000682.1:g.3649619G=	GRCh37
NC_000020.9:g.3597619G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2433C= MANE Select	ENSP00000348912.3:p.Cys811=
ENST00000350009.6:c.2355C=	ENSP00000322550.5:p.Cys785=
ENST00000356518.6:c.2433C=	ENSP00000348912.2:p.Cys811=
ENST00000379861.8:c.2430C=	ENSP00000369190.4:p.Cys810=
ENST00000466620.5:n.1994C=
ENST00000483362.1:n.1356C=
ENST00000617732.1:c.*1117C=	ENSP00000483343.1:n.*1117C=
ENST00000619289.4:c.2070C=	ENSP00000484600.1:p.Cys690=
NM_001282447.1:c.2430C=	NP_001269376.1:p.Cys810=
NM_025220.3:c.2433C=	NP_079496.1:p.Cys811=
NM_153202.2:c.2355C=	NP_694882.1:p.Cys785=
XM_005260843.1:c.2472C=	XP_005260900.1:p.Cys824=
XM_006723639.1:c.2469C=	XP_006723702.1:p.Cys823=
XM_006723640.1:c.2463C=	XP_006723703.1:p.Cys821=
XM_011529366.1:c.2469C=	XP_011527668.1:p.Cys823=
XM_011529367.1:c.2430C=	XP_011527669.1:p.Cys810=
XM_011529368.1:c.2394C=	XP_011527670.1:p.Cys798=
XM_011529373.1:c.1470C=	XP_011527675.1:p.Cys490=
XR_937152.1:n.2481C=
XR_937153.1:n.2454C=
XR_937154.1:n.2454C=
XR_937155.1:n.2375C=
XR_937157.1:n.2377C=
NM_001282447.2:c.2430C=	NP_001269376.1:p.Cys810=
NM_025220.4:c.2433C=	NP_079496.1:p.Cys811=
NM_153202.3:c.2355C=	NP_694882.1:p.Cys785=
XM_011529373.2:c.1470C=	XP_011527675.1:p.Cys490=
XR_001754405.1:n.2541C=
XR_002958534.1:n.2650C=
NM_001282447.3:c.2430C=	NP_001269376.1:p.Cys810=
NM_025220.5:c.2433C= MANE Select	NP_079496.1:p.Cys811=
NM_153202.4:c.2355C=	NP_694882.1:p.Cys785=