Canonical Allele Identifier: CA9745043
Gene: ADAM33 HGNC NCBI

Linked Data

dbSNP Id: rs779600787

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669505T>G , CM000682.2:g.3669505T>G GRCh38
NC_000020.10:g.3650152T>G , CM000682.1:g.3650152T>G GRCh37
NC_000020.9:g.3598152T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2332+41A>C MANE Select ENSP00000348912.3:n.2332+41A>C
ENST00000350009.6:c.2254+41A>C ENSP00000322550.5:n.2254+41A>C
ENST00000356518.6:c.2332+41A>C ENSP00000348912.2:n.2332+41A>C
ENST00000379861.8:c.2332+41A>C ENSP00000369190.4:n.2332+41A>C
ENST00000466620.5:n.1893+41A>C
ENST00000483362.1:n.1121A>C
ENST00000617732.1:c.*1019+41A>C ENSP00000483343.1:n.*1019+41A>C
ENST00000619289.4:c.1972+41A>C ENSP00000484600.1:n.1972+41A>C
NM_001282447.1:c.2332+41A>C NP_001269376.1:n.2332+41A>C
NM_025220.3:c.2332+41A>C NP_079496.1:n.2332+41A>C
NM_153202.2:c.2254+41A>C NP_694882.1:n.2254+41A>C
XM_005260843.1:c.2371+41A>C XP_005260900.1:n.2371+41A>C
XM_006723639.1:c.2371+41A>C XP_006723702.1:n.2371+41A>C
XM_006723640.1:c.2362+41A>C XP_006723703.1:n.2362+41A>C
XM_011529366.1:c.2368+41A>C XP_011527668.1:n.2368+41A>C
XM_011529367.1:c.2329+41A>C XP_011527669.1:n.2329+41A>C
XM_011529368.1:c.2293+41A>C XP_011527670.1:n.2293+41A>C
XM_011529373.1:c.1369+41A>C XP_011527675.1:n.1369+41A>C
XR_937151.1:n.2384-135A>C
XR_937152.1:n.2384-135A>C
XR_937153.1:n.2356+41A>C
XR_937154.1:n.2356+41A>C
XR_937155.1:n.2277+41A>C
XR_937157.1:n.2279+41A>C
NM_001282447.2:c.2332+41A>C NP_001269376.1:n.2332+41A>C
NM_025220.4:c.2332+41A>C NP_079496.1:n.2332+41A>C
NM_153202.3:c.2254+41A>C NP_694882.1:n.2254+41A>C
XM_011529373.2:c.1369+41A>C XP_011527675.1:n.1369+41A>C
XR_001754405.1:n.2443+41A>C
XR_002958534.1:n.2552+41A>C
NM_001282447.3:c.2332+41A>C NP_001269376.1:n.2332+41A>C
NM_025220.5:c.2332+41A>C MANE Select NP_079496.1:n.2332+41A>C
NM_153202.4:c.2254+41A>C NP_694882.1:n.2254+41A>C