Canonical Allele Identifier: CA744011024
Gene: ADAM33 HGNC NCBI

Linked Data

dbSNP Id: rs1458120162

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3668329_3668333del , CM000682.2:g.3668329_3668333del GRCh38
NC_000020.10:g.3648976_3648980del , CM000682.1:g.3648976_3648980del GRCh37
NC_000020.9:g.3596976_3596980del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.*630_*634del MANE Select ENSP00000348912.3:n.*630_*634del
ENST00000350009.6:c.*630_*634del ENSP00000322550.5:n.*630_*634del
ENST00000356518.6:c.*630_*634del ENSP00000348912.2:n.*630_*634del
ENST00000379861.8:c.*630_*634del ENSP00000369190.4:n.*630_*634del
ENST00000466620.5:n.2633_2637del
ENST00000483362.1:n.1995_1999del
ENST00000619289.4:c.*630_*634del ENSP00000484600.1:n.*630_*634del
NM_001282447.1:c.*630_*634del NP_001269376.1:n.*630_*634del
NM_025220.3:c.*630_*634del NP_079496.1:n.*630_*634del
NM_153202.2:c.*630_*634del NP_694882.1:n.*630_*634del
XM_005260843.1:c.*630_*634del XP_005260900.1:n.*630_*634del
XM_006723639.1:c.*630_*634del XP_006723702.1:n.*630_*634del
XM_006723640.1:c.*630_*634del XP_006723703.1:n.*630_*634del
XM_011529366.1:c.*630_*634del XP_011527668.1:n.*630_*634del
XM_011529367.1:c.*630_*634del XP_011527669.1:n.*630_*634del
XM_011529368.1:c.*630_*634del XP_011527670.1:n.*630_*634del
XM_011529373.1:c.*630_*634del XP_011527675.1:n.*630_*634del
XR_937153.1:n.3093_3097del
XR_937154.1:n.3093_3097del
XR_937155.1:n.3014_3018del
XR_937157.1:n.3016_3020del
NM_001282447.2:c.*630_*634del NP_001269376.1:n.*630_*634del
NM_025220.4:c.*630_*634del NP_079496.1:n.*630_*634del
NM_153202.3:c.*630_*634del NP_694882.1:n.*630_*634del
XM_011529373.2:c.*630_*634del XP_011527675.1:n.*630_*634del
XR_001754405.1:n.3180_3184del
XR_002958534.1:n.3289_3293del
NM_001282447.3:c.*630_*634del NP_001269376.1:n.*630_*634del
NM_025220.5:c.*630_*634del MANE Select NP_079496.1:n.*630_*634del
NM_153202.4:c.*630_*634del NP_694882.1:n.*630_*634del