Canonical Allele Identifier: CA2346677151
Gene: ADAM33 HGNC NCBI

Linked Data

dbSNP Id: rs2087334770
gnomAD v4: 20-3668524-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3668524G>C , CM000682.2:g.3668524G>C GRCh38
NC_000020.10:g.3649171G>C , CM000682.1:g.3649171G>C GRCh37
NC_000020.9:g.3597171G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.*439C>G MANE Select ENSP00000348912.3:n.*439C>G
ENST00000350009.6:c.*439C>G ENSP00000322550.5:n.*439C>G
ENST00000356518.6:c.*439C>G ENSP00000348912.2:n.*439C>G
ENST00000379861.8:c.*439C>G ENSP00000369190.4:n.*439C>G
ENST00000466620.5:n.2442C>G
ENST00000483362.1:n.1804C>G
ENST00000619289.4:c.*439C>G ENSP00000484600.1:n.*439C>G
NM_001282447.1:c.*439C>G NP_001269376.1:n.*439C>G
NM_025220.3:c.*439C>G NP_079496.1:n.*439C>G
NM_153202.2:c.*439C>G NP_694882.1:n.*439C>G
XM_005260843.1:c.*439C>G XP_005260900.1:n.*439C>G
XM_006723639.1:c.*439C>G XP_006723702.1:n.*439C>G
XM_006723640.1:c.*439C>G XP_006723703.1:n.*439C>G
XM_011529366.1:c.*439C>G XP_011527668.1:n.*439C>G
XM_011529367.1:c.*439C>G XP_011527669.1:n.*439C>G
XM_011529368.1:c.*439C>G XP_011527670.1:n.*439C>G
XM_011529373.1:c.*439C>G XP_011527675.1:n.*439C>G
XR_937153.1:n.2902C>G
XR_937154.1:n.2902C>G
XR_937155.1:n.2823C>G
XR_937157.1:n.2825C>G
NM_001282447.2:c.*439C>G NP_001269376.1:n.*439C>G
NM_025220.4:c.*439C>G NP_079496.1:n.*439C>G
NM_153202.3:c.*439C>G NP_694882.1:n.*439C>G
XM_011529373.2:c.*439C>G XP_011527675.1:n.*439C>G
XR_001754405.1:n.2989C>G
XR_002958534.1:n.3098C>G
NM_001282447.3:c.*439C>G NP_001269376.1:n.*439C>G
NM_025220.5:c.*439C>G MANE Select NP_079496.1:n.*439C>G
NM_153202.4:c.*439C>G NP_694882.1:n.*439C>G