Canonical Allele Identifier: CA2346677321
Gene: ADAM33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3668841C= , CM000682.2:g.3668841C= GRCh38
NC_000020.10:g.3649488C= , CM000682.1:g.3649488C= GRCh37
NC_000020.9:g.3597488C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.*122G= MANE Select ENSP00000348912.3:n.*122G=
ENST00000350009.6:c.*122G= ENSP00000322550.5:n.*122G=
ENST00000356518.6:c.*122G= ENSP00000348912.2:n.*122G=
ENST00000379861.8:c.*122G= ENSP00000369190.4:n.*122G=
ENST00000466620.5:n.2125G=
ENST00000483362.1:n.1487G=
ENST00000617732.1:c.*1248G= ENSP00000483343.1:n.*1248G=
ENST00000619289.4:c.*122G= ENSP00000484600.1:n.*122G=
NM_001282447.1:c.*122G= NP_001269376.1:n.*122G=
NM_025220.3:c.*122G= NP_079496.1:n.*122G=
NM_153202.2:c.*122G= NP_694882.1:n.*122G=
XM_005260843.1:c.*122G= XP_005260900.1:n.*122G=
XM_006723639.1:c.*122G= XP_006723702.1:n.*122G=
XM_006723640.1:c.*122G= XP_006723703.1:n.*122G=
XM_011529366.1:c.*122G= XP_011527668.1:n.*122G=
XM_011529367.1:c.*122G= XP_011527669.1:n.*122G=
XM_011529368.1:c.*122G= XP_011527670.1:n.*122G=
XM_011529373.1:c.*122G= XP_011527675.1:n.*122G=
XR_937153.1:n.2585G=
XR_937154.1:n.2585G=
XR_937155.1:n.2506G=
XR_937157.1:n.2508G=
NM_001282447.2:c.*122G= NP_001269376.1:n.*122G=
NM_025220.4:c.*122G= NP_079496.1:n.*122G=
NM_153202.3:c.*122G= NP_694882.1:n.*122G=
XM_011529373.2:c.*122G= XP_011527675.1:n.*122G=
XR_001754405.1:n.2672G=
XR_002958534.1:n.2781G=
NM_001282447.3:c.*122G= NP_001269376.1:n.*122G=
NM_025220.5:c.*122G= MANE Select NP_079496.1:n.*122G=
NM_153202.4:c.*122G= NP_694882.1:n.*122G=