Canonical Allele Identifier: CA408103821

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669594G>T , CM000682.2:g.3669594G>T	GRCh38
NC_000020.10:g.3650241G>T , CM000682.1:g.3650241G>T	GRCh37
NC_000020.9:g.3598241G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_025220.5:c.2284C>A MANE Select	NP_079496.1:p.His762Asn
ENST00000356518.7:c.2284C>A MANE Select	ENSP00000348912.3:p.His762Asn
NM_001282447.1:c.2284C>A	NP_001269376.1:p.His762Asn
NM_001282447.2:c.2284C>A	NP_001269376.1:p.His762Asn
NM_001282447.3:c.2284C>A	NP_001269376.1:p.His762Asn
NM_025220.3:c.2284C>A	NP_079496.1:p.His762Asn
NM_025220.4:c.2284C>A	NP_079496.1:p.His762Asn
NM_153202.2:c.2206C>A	NP_694882.1:p.His736Asn
NM_153202.3:c.2206C>A	NP_694882.1:p.His736Asn
NM_153202.4:c.2206C>A	NP_694882.1:p.His736Asn
ENST00000350009.6:c.2206C>A	ENSP00000322550.5:p.His736Asn
ENST00000356518.6:c.2284C>A	ENSP00000348912.2:p.His762Asn
ENST00000379861.8:c.2284C>A	ENSP00000369190.4:p.His762Asn
ENST00000466620.5:n.1845C>A
ENST00000483362.1:n.1032C>A
ENST00000617732.1:c.*971C>A	ENSP00000483343.1:n.*971C>A
ENST00000619289.4:c.1924C>A	ENSP00000484600.1:p.His642Asn
XM_005260843.1:c.2323C>A	XP_005260900.1:p.His775Asn
XM_006723639.1:c.2323C>A	XP_006723702.1:p.His775Asn
XM_006723640.1:c.2314C>A	XP_006723703.1:p.His772Asn
XM_011529366.1:c.2320C>A	XP_011527668.1:p.His774Asn
XM_011529367.1:c.2281C>A	XP_011527669.1:p.His761Asn
XM_011529368.1:c.2245C>A	XP_011527670.1:p.His749Asn
XM_011529373.1:c.1321C>A	XP_011527675.1:p.His441Asn
XM_011529373.2:c.1321C>A	XP_011527675.1:p.His441Asn
XR_001754405.1:n.2395C>A
XR_002958534.1:n.2504C>A
XR_937151.1:n.2384-224C>A
XR_937152.1:n.2384-224C>A
XR_937153.1:n.2308C>A
XR_937154.1:n.2308C>A
XR_937155.1:n.2229C>A
XR_937157.1:n.2231C>A