Canonical Allele Identifier: CA408103805
Gene: ADAM33 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669587A>C , CM000682.2:g.3669587A>C GRCh38
NC_000020.10:g.3650234A>C , CM000682.1:g.3650234A>C GRCh37
NC_000020.9:g.3598234A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2291T>G MANE Select ENSP00000348912.3:p.Met764Arg
ENST00000350009.6:c.2213T>G ENSP00000322550.5:p.Met738Arg
ENST00000356518.6:c.2291T>G ENSP00000348912.2:p.Met764Arg
ENST00000379861.8:c.2291T>G ENSP00000369190.4:p.Met764Arg
ENST00000466620.5:n.1852T>G
ENST00000483362.1:n.1039T>G
ENST00000617732.1:c.*978T>G ENSP00000483343.1:n.*978T>G
ENST00000619289.4:c.1931T>G ENSP00000484600.1:p.Met644Arg
NM_001282447.1:c.2291T>G NP_001269376.1:p.Met764Arg
NM_025220.3:c.2291T>G NP_079496.1:p.Met764Arg
NM_153202.2:c.2213T>G NP_694882.1:p.Met738Arg
XM_005260843.1:c.2330T>G XP_005260900.1:p.Met777Arg
XM_006723639.1:c.2330T>G XP_006723702.1:p.Met777Arg
XM_006723640.1:c.2321T>G XP_006723703.1:p.Met774Arg
XM_011529366.1:c.2327T>G XP_011527668.1:p.Met776Arg
XM_011529367.1:c.2288T>G XP_011527669.1:p.Met763Arg
XM_011529368.1:c.2252T>G XP_011527670.1:p.Met751Arg
XM_011529373.1:c.1328T>G XP_011527675.1:p.Met443Arg
XR_937151.1:n.2384-217T>G
XR_937152.1:n.2384-217T>G
XR_937153.1:n.2315T>G
XR_937154.1:n.2315T>G
XR_937155.1:n.2236T>G
XR_937157.1:n.2238T>G
NM_001282447.2:c.2291T>G NP_001269376.1:p.Met764Arg
NM_025220.4:c.2291T>G NP_079496.1:p.Met764Arg
NM_153202.3:c.2213T>G NP_694882.1:p.Met738Arg
XM_011529373.2:c.1328T>G XP_011527675.1:p.Met443Arg
XR_001754405.1:n.2402T>G
XR_002958534.1:n.2511T>G
NM_001282447.3:c.2291T>G NP_001269376.1:p.Met764Arg
NM_025220.5:c.2291T>G MANE Select NP_079496.1:p.Met764Arg
NM_153202.4:c.2213T>G NP_694882.1:p.Met738Arg