Canonical Allele Identifier: CA920153798
Gene: ADAM33 HGNC NCBI

Linked Data

dbSNP Id: rs1568792223

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3668449_3668450del , CM000682.2:g.3668449_3668450del GRCh38
NC_000020.10:g.3649096_3649097del , CM000682.1:g.3649096_3649097del GRCh37
NC_000020.9:g.3597096_3597097del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.*513_*514del MANE Select ENSP00000348912.3:n.*513_*514del
ENST00000350009.6:c.*513_*514del ENSP00000322550.5:n.*513_*514del
ENST00000356518.6:c.*513_*514del ENSP00000348912.2:n.*513_*514del
ENST00000379861.8:c.*513_*514del ENSP00000369190.4:n.*513_*514del
ENST00000466620.5:n.2516_2517del
ENST00000483362.1:n.1878_1879del
ENST00000619289.4:c.*513_*514del ENSP00000484600.1:n.*513_*514del
NM_001282447.1:c.*513_*514del NP_001269376.1:n.*513_*514del
NM_025220.3:c.*513_*514del NP_079496.1:n.*513_*514del
NM_153202.2:c.*513_*514del NP_694882.1:n.*513_*514del
XM_005260843.1:c.*513_*514del XP_005260900.1:n.*513_*514del
XM_006723639.1:c.*513_*514del XP_006723702.1:n.*513_*514del
XM_006723640.1:c.*513_*514del XP_006723703.1:n.*513_*514del
XM_011529366.1:c.*513_*514del XP_011527668.1:n.*513_*514del
XM_011529367.1:c.*513_*514del XP_011527669.1:n.*513_*514del
XM_011529368.1:c.*513_*514del XP_011527670.1:n.*513_*514del
XM_011529373.1:c.*513_*514del XP_011527675.1:n.*513_*514del
XR_937153.1:n.2976_2977del
XR_937154.1:n.2976_2977del
XR_937155.1:n.2897_2898del
XR_937157.1:n.2899_2900del
NM_001282447.2:c.*513_*514del NP_001269376.1:n.*513_*514del
NM_025220.4:c.*513_*514del NP_079496.1:n.*513_*514del
NM_153202.3:c.*513_*514del NP_694882.1:n.*513_*514del
XM_011529373.2:c.*513_*514del XP_011527675.1:n.*513_*514del
XR_001754405.1:n.3063_3064del
XR_002958534.1:n.3172_3173del
NM_001282447.3:c.*513_*514del NP_001269376.1:n.*513_*514del
NM_025220.5:c.*513_*514del MANE Select NP_079496.1:n.*513_*514del
NM_153202.4:c.*513_*514del NP_694882.1:n.*513_*514del