Canonical Allele Identifier: CA408103822
Gene: ADAM33 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669596A>C , CM000682.2:g.3669596A>C GRCh38
NC_000020.10:g.3650243A>C , CM000682.1:g.3650243A>C GRCh37
NC_000020.9:g.3598243A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2282T>G MANE Select ENSP00000348912.3:p.Val761Gly
ENST00000350009.6:c.2204T>G ENSP00000322550.5:p.Val735Gly
ENST00000356518.6:c.2282T>G ENSP00000348912.2:p.Val761Gly
ENST00000379861.8:c.2282T>G ENSP00000369190.4:p.Val761Gly
ENST00000466620.5:n.1843T>G
ENST00000483362.1:n.1030T>G
ENST00000617732.1:c.*969T>G ENSP00000483343.1:n.*969T>G
ENST00000619289.4:c.1922T>G ENSP00000484600.1:p.Val641Gly
NM_001282447.1:c.2282T>G NP_001269376.1:p.Val761Gly
NM_025220.3:c.2282T>G NP_079496.1:p.Val761Gly
NM_153202.2:c.2204T>G NP_694882.1:p.Val735Gly
XM_005260843.1:c.2321T>G XP_005260900.1:p.Val774Gly
XM_006723639.1:c.2321T>G XP_006723702.1:p.Val774Gly
XM_006723640.1:c.2312T>G XP_006723703.1:p.Val771Gly
XM_011529366.1:c.2318T>G XP_011527668.1:p.Val773Gly
XM_011529367.1:c.2279T>G XP_011527669.1:p.Val760Gly
XM_011529368.1:c.2243T>G XP_011527670.1:p.Val748Gly
XM_011529373.1:c.1319T>G XP_011527675.1:p.Val440Gly
XR_937151.1:n.2384-226T>G
XR_937152.1:n.2384-226T>G
XR_937153.1:n.2306T>G
XR_937154.1:n.2306T>G
XR_937155.1:n.2227T>G
XR_937157.1:n.2229T>G
NM_001282447.2:c.2282T>G NP_001269376.1:p.Val761Gly
NM_025220.4:c.2282T>G NP_079496.1:p.Val761Gly
NM_153202.3:c.2204T>G NP_694882.1:p.Val735Gly
XM_011529373.2:c.1319T>G XP_011527675.1:p.Val440Gly
XR_001754405.1:n.2393T>G
XR_002958534.1:n.2502T>G
NM_001282447.3:c.2282T>G NP_001269376.1:p.Val761Gly
NM_025220.5:c.2282T>G MANE Select NP_079496.1:p.Val761Gly
NM_153202.4:c.2204T>G NP_694882.1:p.Val735Gly