Canonical Allele Identifier: CA634188032
Gene: ADAM33 HGNC NCBI

Linked Data

dbSNP Id: rs1357701742

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3668436_3668437insG , CM000682.2:g.3668436_3668437insG GRCh38
NC_000020.10:g.3649083_3649084insG , CM000682.1:g.3649083_3649084insG GRCh37
NC_000020.9:g.3597083_3597084insG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.*526_*527insC MANE Select ENSP00000348912.3:n.*526_*527insC
ENST00000350009.6:c.*526_*527insC ENSP00000322550.5:n.*526_*527insC
ENST00000356518.6:c.*526_*527insC ENSP00000348912.2:n.*526_*527insC
ENST00000379861.8:c.*526_*527insC ENSP00000369190.4:n.*526_*527insC
ENST00000466620.5:n.2529_2530insC
ENST00000483362.1:n.1891_1892insC
ENST00000619289.4:c.*526_*527insC ENSP00000484600.1:n.*526_*527insC
NM_001282447.1:c.*526_*527insC NP_001269376.1:n.*526_*527insC
NM_025220.3:c.*526_*527insC NP_079496.1:n.*526_*527insC
NM_153202.2:c.*526_*527insC NP_694882.1:n.*526_*527insC
XM_005260843.1:c.*526_*527insC XP_005260900.1:n.*526_*527insC
XM_006723639.1:c.*526_*527insC XP_006723702.1:n.*526_*527insC
XM_006723640.1:c.*526_*527insC XP_006723703.1:n.*526_*527insC
XM_011529366.1:c.*526_*527insC XP_011527668.1:n.*526_*527insC
XM_011529367.1:c.*526_*527insC XP_011527669.1:n.*526_*527insC
XM_011529368.1:c.*526_*527insC XP_011527670.1:n.*526_*527insC
XM_011529373.1:c.*526_*527insC XP_011527675.1:n.*526_*527insC
XR_937153.1:n.2989_2990insC
XR_937154.1:n.2989_2990insC
XR_937155.1:n.2910_2911insC
XR_937157.1:n.2912_2913insC
NM_001282447.2:c.*526_*527insC NP_001269376.1:n.*526_*527insC
NM_025220.4:c.*526_*527insC NP_079496.1:n.*526_*527insC
NM_153202.3:c.*526_*527insC NP_694882.1:n.*526_*527insC
XM_011529373.2:c.*526_*527insC XP_011527675.1:n.*526_*527insC
XR_001754405.1:n.3076_3077insC
XR_002958534.1:n.3185_3186insC
NM_001282447.3:c.*526_*527insC NP_001269376.1:n.*526_*527insC
NM_025220.5:c.*526_*527insC MANE Select NP_079496.1:n.*526_*527insC
NM_153202.4:c.*526_*527insC NP_694882.1:n.*526_*527insC