Canonical Allele Identifier: CA2651722759
Gene: ADAM33 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3668417del , CM000682.2:g.3668417del GRCh38
NC_000020.10:g.3649064del , CM000682.1:g.3649064del GRCh37
NC_000020.9:g.3597064del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.*546del MANE Select ENSP00000348912.3:n.*546del
ENST00000350009.6:c.*546del ENSP00000322550.5:n.*546del
ENST00000356518.6:c.*546del ENSP00000348912.2:n.*546del
ENST00000379861.8:c.*546del ENSP00000369190.4:n.*546del
ENST00000466620.5:n.2549del
ENST00000483362.1:n.1911del
ENST00000619289.4:c.*546del ENSP00000484600.1:n.*546del
NM_001282447.1:c.*546del NP_001269376.1:n.*546del
NM_025220.3:c.*546del NP_079496.1:n.*546del
NM_153202.2:c.*546del NP_694882.1:n.*546del
XM_005260843.1:c.*546del XP_005260900.1:n.*546del
XM_006723639.1:c.*546del XP_006723702.1:n.*546del
XM_006723640.1:c.*546del XP_006723703.1:n.*546del
XM_011529366.1:c.*546del XP_011527668.1:n.*546del
XM_011529367.1:c.*546del XP_011527669.1:n.*546del
XM_011529368.1:c.*546del XP_011527670.1:n.*546del
XM_011529373.1:c.*546del XP_011527675.1:n.*546del
XR_937153.1:n.3009del
XR_937154.1:n.3009del
XR_937155.1:n.2930del
XR_937157.1:n.2932del
NM_001282447.2:c.*546del NP_001269376.1:n.*546del
NM_025220.4:c.*546del NP_079496.1:n.*546del
NM_153202.3:c.*546del NP_694882.1:n.*546del
XM_011529373.2:c.*546del XP_011527675.1:n.*546del
XR_001754405.1:n.3096del
XR_002958534.1:n.3205del
NM_001282447.3:c.*546del NP_001269376.1:n.*546del
NM_025220.5:c.*546del MANE Select NP_079496.1:n.*546del
NM_153202.4:c.*546del NP_694882.1:n.*546del