Canonical Allele Identifier: CA2346677071
Gene: ADAM33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3668365G= , CM000682.2:g.3668365G= GRCh38
NC_000020.10:g.3649012G= , CM000682.1:g.3649012G= GRCh37
NC_000020.9:g.3597012G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.*598C= MANE Select ENSP00000348912.3:n.*598C=
ENST00000350009.6:c.*598C= ENSP00000322550.5:n.*598C=
ENST00000356518.6:c.*598C= ENSP00000348912.2:n.*598C=
ENST00000379861.8:c.*598C= ENSP00000369190.4:n.*598C=
ENST00000466620.5:n.2601C=
ENST00000483362.1:n.1963C=
ENST00000619289.4:c.*598C= ENSP00000484600.1:n.*598C=
NM_001282447.1:c.*598C= NP_001269376.1:n.*598C=
NM_025220.3:c.*598C= NP_079496.1:n.*598C=
NM_153202.2:c.*598C= NP_694882.1:n.*598C=
XM_005260843.1:c.*598C= XP_005260900.1:n.*598C=
XM_006723639.1:c.*598C= XP_006723702.1:n.*598C=
XM_006723640.1:c.*598C= XP_006723703.1:n.*598C=
XM_011529366.1:c.*598C= XP_011527668.1:n.*598C=
XM_011529367.1:c.*598C= XP_011527669.1:n.*598C=
XM_011529368.1:c.*598C= XP_011527670.1:n.*598C=
XM_011529373.1:c.*598C= XP_011527675.1:n.*598C=
XR_937153.1:n.3061C=
XR_937154.1:n.3061C=
XR_937155.1:n.2982C=
XR_937157.1:n.2984C=
NM_001282447.2:c.*598C= NP_001269376.1:n.*598C=
NM_025220.4:c.*598C= NP_079496.1:n.*598C=
NM_153202.3:c.*598C= NP_694882.1:n.*598C=
XM_011529373.2:c.*598C= XP_011527675.1:n.*598C=
XR_001754405.1:n.3148C=
XR_002958534.1:n.3257C=
NM_001282447.3:c.*598C= NP_001269376.1:n.*598C=
NM_025220.5:c.*598C= MANE Select NP_079496.1:n.*598C=
NM_153202.4:c.*598C= NP_694882.1:n.*598C=