Canonical Allele Identifier: CA310997842
Gene: ADAM33 HGNC NCBI

Linked Data

dbSNP Id: rs1023941211

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3670288dup , CM000682.2:g.3670288dup GRCh38
NC_000020.10:g.3650935dup , CM000682.1:g.3650935dup GRCh37
NC_000020.9:g.3598935dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356518.7:c.2241-651dup MANE Select ENSP00000348912.3:n.2241-651dup
ENST00000350009.6:c.2163-651dup ENSP00000322550.5:n.2163-651dup
ENST00000356518.6:c.2241-651dup ENSP00000348912.2:n.2241-651dup
ENST00000379861.8:c.2241-651dup ENSP00000369190.4:n.2241-651dup
ENST00000466620.5:n.1802-651dup
ENST00000483362.1:n.338dup
ENST00000617732.1:c.*928-651dup ENSP00000483343.1:n.*928-651dup
ENST00000619289.4:c.1881-651dup ENSP00000484600.1:n.1881-651dup
NM_001282447.1:c.2241-651dup NP_001269376.1:n.2241-651dup
NM_025220.3:c.2241-651dup NP_079496.1:n.2241-651dup
NM_153202.2:c.2163-651dup NP_694882.1:n.2163-651dup
XM_005260843.1:c.2280-651dup XP_005260900.1:n.2280-651dup
XM_006723639.1:c.2280-651dup XP_006723702.1:n.2280-651dup
XM_006723640.1:c.2271-651dup XP_006723703.1:n.2271-651dup
XM_011529366.1:c.2277-651dup XP_011527668.1:n.2277-651dup
XM_011529367.1:c.2238-651dup XP_011527669.1:n.2238-651dup
XM_011529368.1:c.2202-651dup XP_011527670.1:n.2202-651dup
XM_011529373.1:c.1278-651dup XP_011527675.1:n.1278-651dup
XR_937151.1:n.2383+718dup
XR_937152.1:n.2383+718dup
XR_937153.1:n.2265-651dup
XR_937154.1:n.2265-651dup
XR_937155.1:n.2186-651dup
XR_937157.1:n.2188-651dup
NM_001282447.2:c.2241-651dup NP_001269376.1:n.2241-651dup
NM_025220.4:c.2241-651dup NP_079496.1:n.2241-651dup
NM_153202.3:c.2163-651dup NP_694882.1:n.2163-651dup
XM_011529373.2:c.1278-651dup XP_011527675.1:n.1278-651dup
XR_001754405.1:n.2352-651dup
XR_002958534.1:n.2461-651dup
NM_001282447.3:c.2241-651dup NP_001269376.1:n.2241-651dup
NM_025220.5:c.2241-651dup MANE Select NP_079496.1:n.2241-651dup
NM_153202.4:c.2163-651dup NP_694882.1:n.2163-651dup