Canonical Allele Identifier: CA2346677169
Gene: ADAM33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3668557A= , CM000682.2:g.3668557A= GRCh38
NC_000020.10:g.3649204A= , CM000682.1:g.3649204A= GRCh37
NC_000020.9:g.3597204A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.*406T= MANE Select ENSP00000348912.3:n.*406T=
ENST00000350009.6:c.*406T= ENSP00000322550.5:n.*406T=
ENST00000356518.6:c.*406T= ENSP00000348912.2:n.*406T=
ENST00000379861.8:c.*406T= ENSP00000369190.4:n.*406T=
ENST00000466620.5:n.2409T=
ENST00000483362.1:n.1771T=
ENST00000619289.4:c.*406T= ENSP00000484600.1:n.*406T=
NM_001282447.1:c.*406T= NP_001269376.1:n.*406T=
NM_025220.3:c.*406T= NP_079496.1:n.*406T=
NM_153202.2:c.*406T= NP_694882.1:n.*406T=
XM_005260843.1:c.*406T= XP_005260900.1:n.*406T=
XM_006723639.1:c.*406T= XP_006723702.1:n.*406T=
XM_006723640.1:c.*406T= XP_006723703.1:n.*406T=
XM_011529366.1:c.*406T= XP_011527668.1:n.*406T=
XM_011529367.1:c.*406T= XP_011527669.1:n.*406T=
XM_011529368.1:c.*406T= XP_011527670.1:n.*406T=
XM_011529373.1:c.*406T= XP_011527675.1:n.*406T=
XR_937153.1:n.2869T=
XR_937154.1:n.2869T=
XR_937155.1:n.2790T=
XR_937157.1:n.2792T=
NM_001282447.2:c.*406T= NP_001269376.1:n.*406T=
NM_025220.4:c.*406T= NP_079496.1:n.*406T=
NM_153202.3:c.*406T= NP_694882.1:n.*406T=
XM_011529373.2:c.*406T= XP_011527675.1:n.*406T=
XR_001754405.1:n.2956T=
XR_002958534.1:n.3065T=
NM_001282447.3:c.*406T= NP_001269376.1:n.*406T=
NM_025220.5:c.*406T= MANE Select NP_079496.1:n.*406T=
NM_153202.4:c.*406T= NP_694882.1:n.*406T=