Canonical Allele Identifier: CA2346677119
Gene: ADAM33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3668461_3668463delinsAAC , CM000682.2:g.3668461_3668463delinsAAC GRCh38
NC_000020.10:g.3649108_3649110delinsAAC , CM000682.1:g.3649108_3649110delinsAAC GRCh37
NC_000020.9:g.3597108_3597110delinsAAC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.*500_*502delinsGTT MANE Select ENSP00000348912.3:n.*500_*502delinsGTT
ENST00000350009.6:c.*500_*502delinsGTT ENSP00000322550.5:n.*500_*502delinsGTT
ENST00000356518.6:c.*500_*502delinsGTT ENSP00000348912.2:n.*500_*502delinsGTT
ENST00000379861.8:c.*500_*502delinsGTT ENSP00000369190.4:n.*500_*502delinsGTT
ENST00000466620.5:n.2503_2505delinsGTT
ENST00000483362.1:n.1865_1867delinsGTT
ENST00000619289.4:c.*500_*502delinsGTT ENSP00000484600.1:n.*500_*502delinsGTT
NM_001282447.1:c.*500_*502delinsGTT NP_001269376.1:n.*500_*502delinsGTT
NM_025220.3:c.*500_*502delinsGTT NP_079496.1:n.*500_*502delinsGTT
NM_153202.2:c.*500_*502delinsGTT NP_694882.1:n.*500_*502delinsGTT
XM_005260843.1:c.*500_*502delinsGTT XP_005260900.1:n.*500_*502delinsGTT
XM_006723639.1:c.*500_*502delinsGTT XP_006723702.1:n.*500_*502delinsGTT
XM_006723640.1:c.*500_*502delinsGTT XP_006723703.1:n.*500_*502delinsGTT
XM_011529366.1:c.*500_*502delinsGTT XP_011527668.1:n.*500_*502delinsGTT
XM_011529367.1:c.*500_*502delinsGTT XP_011527669.1:n.*500_*502delinsGTT
XM_011529368.1:c.*500_*502delinsGTT XP_011527670.1:n.*500_*502delinsGTT
XM_011529373.1:c.*500_*502delinsGTT XP_011527675.1:n.*500_*502delinsGTT
XR_937153.1:n.2963_2965delinsGTT
XR_937154.1:n.2963_2965delinsGTT
XR_937155.1:n.2884_2886delinsGTT
XR_937157.1:n.2886_2888delinsGTT
NM_001282447.2:c.*500_*502delinsGTT NP_001269376.1:n.*500_*502delinsGTT
NM_025220.4:c.*500_*502delinsGTT NP_079496.1:n.*500_*502delinsGTT
NM_153202.3:c.*500_*502delinsGTT NP_694882.1:n.*500_*502delinsGTT
XM_011529373.2:c.*500_*502delinsGTT XP_011527675.1:n.*500_*502delinsGTT
XR_001754405.1:n.3050_3052delinsGTT
XR_002958534.1:n.3159_3161delinsGTT
NM_001282447.3:c.*500_*502delinsGTT NP_001269376.1:n.*500_*502delinsGTT
NM_025220.5:c.*500_*502delinsGTT MANE Select NP_079496.1:n.*500_*502delinsGTT
NM_153202.4:c.*500_*502delinsGTT NP_694882.1:n.*500_*502delinsGTT