Canonical Allele Identifier: CA634329892
Gene: ADAM33 HGNC NCBI

Linked Data

dbSNP Id: rs774282043

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3671801dup , CM000682.2:g.3671801dup GRCh38
NC_000020.10:g.3652448dup , CM000682.1:g.3652448dup GRCh37
NC_000020.9:g.3600448dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356518.7:c.1707-17dup MANE Select ENSP00000348912.3:n.1707-17dup
ENST00000350009.6:c.1707-17dup ENSP00000322550.5:n.1707-17dup
ENST00000356518.6:c.1707-17dup ENSP00000348912.2:n.1707-17dup
ENST00000379861.8:c.1707-17dup ENSP00000369190.4:n.1707-17dup
ENST00000466620.5:n.1346-17dup
ENST00000617732.1:c.*632-339dup ENSP00000483343.1:n.*632-339dup
ENST00000619289.4:c.1347-17dup ENSP00000484600.1:n.1347-17dup
NM_001282447.1:c.1707-17dup NP_001269376.1:n.1707-17dup
NM_025220.3:c.1707-17dup NP_079496.1:n.1707-17dup
NM_153202.2:c.1707-17dup NP_694882.1:n.1707-17dup
XM_005260843.1:c.1746-17dup XP_005260900.1:n.1746-17dup
XM_006723639.1:c.1746-17dup XP_006723702.1:n.1746-17dup
XM_006723640.1:c.1737-17dup XP_006723703.1:n.1737-17dup
XM_011529366.1:c.1743-17dup XP_011527668.1:n.1743-17dup
XM_011529367.1:c.1704-17dup XP_011527669.1:n.1704-17dup
XM_011529368.1:c.1746-17dup XP_011527670.1:n.1746-17dup
XM_011529369.1:c.1714-17dup XP_011527671.1:n.1714-17dup
XM_011529370.1:c.1714-17dup XP_011527672.1:n.1714-17dup
XM_011529373.1:c.744-17dup XP_011527675.1:n.744-17dup
XR_937151.1:n.1850-17dup
XR_937152.1:n.1850-17dup
XR_937153.1:n.1731-17dup
XR_937154.1:n.1731-17dup
XR_937155.1:n.1652-17dup
XR_937157.1:n.1654-17dup
NM_001282447.2:c.1707-17dup NP_001269376.1:n.1707-17dup
NM_025220.4:c.1707-17dup NP_079496.1:n.1707-17dup
NM_153202.3:c.1707-17dup NP_694882.1:n.1707-17dup
XM_011529373.2:c.744-17dup XP_011527675.1:n.744-17dup
XR_001754405.1:n.1818-17dup
XR_002958534.1:n.1927-17dup
NM_001282447.3:c.1707-17dup NP_001269376.1:n.1707-17dup
NM_025220.5:c.1707-17dup MANE Select NP_079496.1:n.1707-17dup
NM_153202.4:c.1707-17dup NP_694882.1:n.1707-17dup