Canonical Allele Identifier: CA2346678081
Gene: ADAM33 HGNC NCBI

Linked Data

dbSNP Id: rs2087449652
gnomAD v3: 20-3670311-A-C
gnomAD v4: 20-3670311-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3670311A>C , CM000682.2:g.3670311A>C GRCh38
NC_000020.10:g.3650958A>C , CM000682.1:g.3650958A>C GRCh37
NC_000020.9:g.3598958A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2241-674T>G MANE Select ENSP00000348912.3:n.2241-674T>G
ENST00000350009.6:c.2163-674T>G ENSP00000322550.5:n.2163-674T>G
ENST00000356518.6:c.2241-674T>G ENSP00000348912.2:n.2241-674T>G
ENST00000379861.8:c.2241-674T>G ENSP00000369190.4:n.2241-674T>G
ENST00000466620.5:n.1802-674T>G
ENST00000483362.1:n.315T>G
ENST00000617732.1:c.*928-674T>G ENSP00000483343.1:n.*928-674T>G
ENST00000619289.4:c.1881-674T>G ENSP00000484600.1:n.1881-674T>G
NM_001282447.1:c.2241-674T>G NP_001269376.1:n.2241-674T>G
NM_025220.3:c.2241-674T>G NP_079496.1:n.2241-674T>G
NM_153202.2:c.2163-674T>G NP_694882.1:n.2163-674T>G
XM_005260843.1:c.2280-674T>G XP_005260900.1:n.2280-674T>G
XM_006723639.1:c.2280-674T>G XP_006723702.1:n.2280-674T>G
XM_006723640.1:c.2271-674T>G XP_006723703.1:n.2271-674T>G
XM_011529366.1:c.2277-674T>G XP_011527668.1:n.2277-674T>G
XM_011529367.1:c.2238-674T>G XP_011527669.1:n.2238-674T>G
XM_011529368.1:c.2202-674T>G XP_011527670.1:n.2202-674T>G
XM_011529373.1:c.1278-674T>G XP_011527675.1:n.1278-674T>G
XR_937151.1:n.2383+695T>G
XR_937152.1:n.2383+695T>G
XR_937153.1:n.2265-674T>G
XR_937154.1:n.2265-674T>G
XR_937155.1:n.2186-674T>G
XR_937157.1:n.2188-674T>G
NM_001282447.2:c.2241-674T>G NP_001269376.1:n.2241-674T>G
NM_025220.4:c.2241-674T>G NP_079496.1:n.2241-674T>G
NM_153202.3:c.2163-674T>G NP_694882.1:n.2163-674T>G
XM_011529373.2:c.1278-674T>G XP_011527675.1:n.1278-674T>G
XR_001754405.1:n.2352-674T>G
XR_002958534.1:n.2461-674T>G
NM_001282447.3:c.2241-674T>G NP_001269376.1:n.2241-674T>G
NM_025220.5:c.2241-674T>G MANE Select NP_079496.1:n.2241-674T>G
NM_153202.4:c.2163-674T>G NP_694882.1:n.2163-674T>G