Canonical Allele Identifier: CA2346679924

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3673661G= , CM000682.2:g.3673661G=	GRCh38
NC_000020.10:g.3654308G= , CM000682.1:g.3654308G=	GRCh37
NC_000020.9:g.3602308G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.906-3C= MANE Select	ENSP00000348912.3:n.906-3C=
ENST00000350009.6:c.906-3C=	ENSP00000322550.5:n.906-3C=
ENST00000356518.6:c.906-3C=	ENSP00000348912.2:n.906-3C=
ENST00000379861.8:c.906-3C=	ENSP00000369190.4:n.906-3C=
ENST00000466620.5:n.87C=
ENST00000617732.1:c.*631+651C=	ENSP00000483343.1:n.*631+651C=
ENST00000619289.4:c.806+183C=	ENSP00000484600.1:n.806+183C=
NM_001282447.1:c.906-3C=	NP_001269376.1:n.906-3C=
NM_025220.3:c.906-3C=	NP_079496.1:n.906-3C=
NM_153202.2:c.906-3C=	NP_694882.1:n.906-3C=
XM_005260843.1:c.945-3C=	XP_005260900.1:n.945-3C=
XM_006723639.1:c.945-3C=	XP_006723702.1:n.945-3C=
XM_006723640.1:c.945-3C=	XP_006723703.1:n.945-3C=
XM_006723644.2:c.945-3C=	XP_006723707.1:n.945-3C=
XM_011529366.1:c.942-3C=	XP_011527668.1:n.942-3C=
XM_011529367.1:c.903-3C=	XP_011527669.1:n.903-3C=
XM_011529368.1:c.945-3C=	XP_011527670.1:n.945-3C=
XM_011529369.1:c.945-3C=	XP_011527671.1:n.945-3C=
XM_011529370.1:c.945-3C=	XP_011527672.1:n.945-3C=
XM_011529371.1:c.945-3C=	XP_011527673.1:n.945-3C=
XM_011529372.1:c.945-3C=	XP_011527674.1:n.945-3C=
XM_011529373.1:c.-52C=	XP_011527675.1:n.-52C=
XR_937151.1:n.1049-3C=
XR_937152.1:n.1049-3C=
XR_937153.1:n.1049-3C=
XR_937154.1:n.1132C=
XR_937155.1:n.1053C=
XR_937157.1:n.1049-3C=
NM_001282447.2:c.906-3C=	NP_001269376.1:n.906-3C=
NM_025220.4:c.906-3C=	NP_079496.1:n.906-3C=
NM_153202.3:c.906-3C=	NP_694882.1:n.906-3C=
XM_011529371.2:c.945-3C=	XP_011527673.1:n.945-3C=
XM_011529373.2:c.-52C=	XP_011527675.1:n.-52C=
XM_017028080.2:c.1028C=	XP_016883569.1:p.Pro343=
XM_017028081.2:c.989C=	XP_016883570.1:p.Pro330=
XM_017028082.1:c.945-3C=	XP_016883571.1:n.945-3C=
XM_017028083.1:c.945-3C=	XP_016883572.1:n.945-3C=
XR_001754405.1:n.1049-3C=
XR_002958534.1:n.1049-3C=
NM_001282447.3:c.906-3C=	NP_001269376.1:n.906-3C=
NM_025220.5:c.906-3C= MANE Select	NP_079496.1:n.906-3C=
NM_153202.4:c.906-3C=	NP_694882.1:n.906-3C=