Canonical Allele Identifier: CA634329895
Gene: ADAM33 HGNC NCBI

Linked Data

dbSNP Id: rs1568800050
MyVariant Identifiers: chr20:g.3652464del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3671822del , CM000682.2:g.3671822del GRCh38
NC_000020.10:g.3652469del , CM000682.1:g.3652469del GRCh37
NC_000020.9:g.3600469del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356518.7:c.1707-38del MANE Select ENSP00000348912.3:n.1707-38del
ENST00000350009.6:c.1707-38del ENSP00000322550.5:n.1707-38del
ENST00000356518.6:c.1707-38del ENSP00000348912.2:n.1707-38del
ENST00000379861.8:c.1707-38del ENSP00000369190.4:n.1707-38del
ENST00000466620.5:n.1346-38del
ENST00000617732.1:c.*632-360del ENSP00000483343.1:n.*632-360del
ENST00000619289.4:c.1347-38del ENSP00000484600.1:n.1347-38del
NM_001282447.1:c.1707-38del NP_001269376.1:n.1707-38del
NM_025220.3:c.1707-38del NP_079496.1:n.1707-38del
NM_153202.2:c.1707-38del NP_694882.1:n.1707-38del
XM_005260843.1:c.1746-38del XP_005260900.1:n.1746-38del
XM_006723639.1:c.1746-38del XP_006723702.1:n.1746-38del
XM_006723640.1:c.1737-38del XP_006723703.1:n.1737-38del
XM_011529366.1:c.1743-38del XP_011527668.1:n.1743-38del
XM_011529367.1:c.1704-38del XP_011527669.1:n.1704-38del
XM_011529368.1:c.1746-38del XP_011527670.1:n.1746-38del
XM_011529369.1:c.1714-38del XP_011527671.1:n.1714-38del
XM_011529370.1:c.1714-38del XP_011527672.1:n.1714-38del
XM_011529373.1:c.744-38del XP_011527675.1:n.744-38del
XR_937151.1:n.1850-38del
XR_937152.1:n.1850-38del
XR_937153.1:n.1731-38del
XR_937154.1:n.1731-38del
XR_937155.1:n.1652-38del
XR_937157.1:n.1654-38del
NM_001282447.2:c.1707-38del NP_001269376.1:n.1707-38del
NM_025220.4:c.1707-38del NP_079496.1:n.1707-38del
NM_153202.3:c.1707-38del NP_694882.1:n.1707-38del
XM_011529373.2:c.744-38del XP_011527675.1:n.744-38del
XR_001754405.1:n.1818-38del
XR_002958534.1:n.1927-38del
NM_001282447.3:c.1707-38del NP_001269376.1:n.1707-38del
NM_025220.5:c.1707-38del MANE Select NP_079496.1:n.1707-38del
NM_153202.4:c.1707-38del NP_694882.1:n.1707-38del