Canonical Allele Identifier: CA9745224
Gene: ADAM33 HGNC NCBI

Linked Data

dbSNP Id: rs775392694

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3671571_3671574dup , CM000682.2:g.3671571_3671574dup GRCh38
NC_000020.10:g.3652218_3652221dup , CM000682.1:g.3652218_3652221dup GRCh37
NC_000020.9:g.3600218_3600221dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.1905+7_1905+10dup MANE Select ENSP00000348912.3:n.1905+7_1905+10dup
ENST00000350009.6:c.1905+7_1905+10dup ENSP00000322550.5:n.1905+7_1905+10dup
ENST00000356518.6:c.1905+7_1905+10dup ENSP00000348912.2:n.1905+7_1905+10dup
ENST00000379861.8:c.1905+7_1905+10dup ENSP00000369190.4:n.1905+7_1905+10dup
ENST00000466620.5:n.1544+7_1544+10dup
ENST00000617732.1:c.*632-117_*632-114dup ENSP00000483343.1:n.*632-117_*632-114dup
ENST00000619289.4:c.1545+7_1545+10dup ENSP00000484600.1:n.1545+7_1545+10dup
NM_001282447.1:c.1905+7_1905+10dup NP_001269376.1:n.1905+7_1905+10dup
NM_025220.3:c.1905+7_1905+10dup NP_079496.1:n.1905+7_1905+10dup
NM_153202.2:c.1905+7_1905+10dup NP_694882.1:n.1905+7_1905+10dup
XM_005260843.1:c.1944+7_1944+10dup XP_005260900.1:n.1944+7_1944+10dup
XM_006723639.1:c.1944+7_1944+10dup XP_006723702.1:n.1944+7_1944+10dup
XM_006723640.1:c.1935+7_1935+10dup XP_006723703.1:n.1935+7_1935+10dup
XM_011529366.1:c.1941+7_1941+10dup XP_011527668.1:n.1941+7_1941+10dup
XM_011529367.1:c.1902+7_1902+10dup XP_011527669.1:n.1902+7_1902+10dup
XM_011529368.1:c.1944+7_1944+10dup XP_011527670.1:n.1944+7_1944+10dup
XM_011529369.1:c.*4+7_*4+10dup XP_011527671.1:n.*4+7_*4+10dup
XM_011529370.1:c.*4+7_*4+10dup XP_011527672.1:n.*4+7_*4+10dup
XM_011529373.1:c.942+7_942+10dup XP_011527675.1:n.942+7_942+10dup
XR_937151.1:n.2048+7_2048+10dup
XR_937152.1:n.2048+7_2048+10dup
XR_937153.1:n.1929+7_1929+10dup
XR_937154.1:n.1929+7_1929+10dup
XR_937155.1:n.1850+7_1850+10dup
XR_937157.1:n.1852+7_1852+10dup
NM_001282447.2:c.1905+7_1905+10dup NP_001269376.1:n.1905+7_1905+10dup
NM_025220.4:c.1905+7_1905+10dup NP_079496.1:n.1905+7_1905+10dup
NM_153202.3:c.1905+7_1905+10dup NP_694882.1:n.1905+7_1905+10dup
XM_011529373.2:c.942+7_942+10dup XP_011527675.1:n.942+7_942+10dup
XR_001754405.1:n.2016+7_2016+10dup
XR_002958534.1:n.2125+7_2125+10dup
NM_001282447.3:c.1905+7_1905+10dup NP_001269376.1:n.1905+7_1905+10dup
NM_025220.5:c.1905+7_1905+10dup MANE Select NP_079496.1:n.1905+7_1905+10dup
NM_153202.4:c.1905+7_1905+10dup NP_694882.1:n.1905+7_1905+10dup