Canonical Allele Identifier: CA2346677613

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669407G= , CM000682.2:g.3669407G=	GRCh38
NC_000020.10:g.3650054G= , CM000682.1:g.3650054G=	GRCh37
NC_000020.9:g.3598054G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2333-37C= MANE Select	ENSP00000348912.3:n.2333-37C=
ENST00000350009.6:c.2255-37C=	ENSP00000322550.5:n.2255-37C=
ENST00000356518.6:c.2333-37C=	ENSP00000348912.2:n.2333-37C=
ENST00000379861.8:c.2333-37C=	ENSP00000369190.4:n.2333-37C=
ENST00000466620.5:n.1894-37C=
ENST00000483362.1:n.1219C=
ENST00000617732.1:c.*1020-37C=	ENSP00000483343.1:n.*1020-37C=
ENST00000619289.4:c.1973-37C=	ENSP00000484600.1:n.1973-37C=
NM_001282447.1:c.2333-37C=	NP_001269376.1:n.2333-37C=
NM_025220.3:c.2333-37C=	NP_079496.1:n.2333-37C=
NM_153202.2:c.2255-37C=	NP_694882.1:n.2255-37C=
XM_005260843.1:c.2372-37C=	XP_005260900.1:n.2372-37C=
XM_006723639.1:c.2372-37C=	XP_006723702.1:n.2372-37C=
XM_006723640.1:c.2363-37C=	XP_006723703.1:n.2363-37C=
XM_011529366.1:c.2369-37C=	XP_011527668.1:n.2369-37C=
XM_011529367.1:c.2330-37C=	XP_011527669.1:n.2330-37C=
XM_011529368.1:c.2294-37C=	XP_011527670.1:n.2294-37C=
XM_011529373.1:c.1370-37C=	XP_011527675.1:n.1370-37C=
XR_937151.1:n.2384-37C=
XR_937152.1:n.2384-37C=
XR_937153.1:n.2357-37C=
XR_937154.1:n.2357-37C=
XR_937155.1:n.2278-37C=
XR_937157.1:n.2280-37C=
NM_001282447.2:c.2333-37C=	NP_001269376.1:n.2333-37C=
NM_025220.4:c.2333-37C=	NP_079496.1:n.2333-37C=
NM_153202.3:c.2255-37C=	NP_694882.1:n.2255-37C=
XM_011529373.2:c.1370-37C=	XP_011527675.1:n.1370-37C=
XR_001754405.1:n.2444-37C=
XR_002958534.1:n.2553-37C=
NM_001282447.3:c.2333-37C=	NP_001269376.1:n.2333-37C=
NM_025220.5:c.2333-37C= MANE Select	NP_079496.1:n.2333-37C=
NM_153202.4:c.2255-37C=	NP_694882.1:n.2255-37C=