Canonical Allele Identifier: CA9745062
Gene: ADAM33 HGNC NCBI

Linked Data

dbSNP Id: rs376337160

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669588T>C , CM000682.2:g.3669588T>C GRCh38
NC_000020.10:g.3650235T>C , CM000682.1:g.3650235T>C GRCh37
NC_000020.9:g.3598235T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2290A>G MANE Select ENSP00000348912.3:p.Met764Val
ENST00000350009.6:c.2212A>G ENSP00000322550.5:p.Met738Val
ENST00000356518.6:c.2290A>G ENSP00000348912.2:p.Met764Val
ENST00000379861.8:c.2290A>G ENSP00000369190.4:p.Met764Val
ENST00000466620.5:n.1851A>G
ENST00000483362.1:n.1038A>G
ENST00000617732.1:c.*977A>G ENSP00000483343.1:n.*977A>G
ENST00000619289.4:c.1930A>G ENSP00000484600.1:p.Met644Val
NM_001282447.1:c.2290A>G NP_001269376.1:p.Met764Val
NM_025220.3:c.2290A>G NP_079496.1:p.Met764Val
NM_153202.2:c.2212A>G NP_694882.1:p.Met738Val
XM_005260843.1:c.2329A>G XP_005260900.1:p.Met777Val
XM_006723639.1:c.2329A>G XP_006723702.1:p.Met777Val
XM_006723640.1:c.2320A>G XP_006723703.1:p.Met774Val
XM_011529366.1:c.2326A>G XP_011527668.1:p.Met776Val
XM_011529367.1:c.2287A>G XP_011527669.1:p.Met763Val
XM_011529368.1:c.2251A>G XP_011527670.1:p.Met751Val
XM_011529373.1:c.1327A>G XP_011527675.1:p.Met443Val
XR_937151.1:n.2384-218A>G
XR_937152.1:n.2384-218A>G
XR_937153.1:n.2314A>G
XR_937154.1:n.2314A>G
XR_937155.1:n.2235A>G
XR_937157.1:n.2237A>G
NM_001282447.2:c.2290A>G NP_001269376.1:p.Met764Val
NM_025220.4:c.2290A>G NP_079496.1:p.Met764Val
NM_153202.3:c.2212A>G NP_694882.1:p.Met738Val
XM_011529373.2:c.1327A>G XP_011527675.1:p.Met443Val
XR_001754405.1:n.2401A>G
XR_002958534.1:n.2510A>G
NM_001282447.3:c.2290A>G NP_001269376.1:p.Met764Val
NM_025220.5:c.2290A>G MANE Select NP_079496.1:p.Met764Val
NM_153202.4:c.2212A>G NP_694882.1:p.Met738Val