Canonical Allele Identifier: CA408103817
Gene: ADAM33 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669593T>G , CM000682.2:g.3669593T>G GRCh38
NC_000020.10:g.3650240T>G , CM000682.1:g.3650240T>G GRCh37
NC_000020.9:g.3598240T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2285A>C MANE Select ENSP00000348912.3:p.His762Pro
ENST00000350009.6:c.2207A>C ENSP00000322550.5:p.His736Pro
ENST00000356518.6:c.2285A>C ENSP00000348912.2:p.His762Pro
ENST00000379861.8:c.2285A>C ENSP00000369190.4:p.His762Pro
ENST00000466620.5:n.1846A>C
ENST00000483362.1:n.1033A>C
ENST00000617732.1:c.*972A>C ENSP00000483343.1:n.*972A>C
ENST00000619289.4:c.1925A>C ENSP00000484600.1:p.His642Pro
NM_001282447.1:c.2285A>C NP_001269376.1:p.His762Pro
NM_025220.3:c.2285A>C NP_079496.1:p.His762Pro
NM_153202.2:c.2207A>C NP_694882.1:p.His736Pro
XM_005260843.1:c.2324A>C XP_005260900.1:p.His775Pro
XM_006723639.1:c.2324A>C XP_006723702.1:p.His775Pro
XM_006723640.1:c.2315A>C XP_006723703.1:p.His772Pro
XM_011529366.1:c.2321A>C XP_011527668.1:p.His774Pro
XM_011529367.1:c.2282A>C XP_011527669.1:p.His761Pro
XM_011529368.1:c.2246A>C XP_011527670.1:p.His749Pro
XM_011529373.1:c.1322A>C XP_011527675.1:p.His441Pro
XR_937151.1:n.2384-223A>C
XR_937152.1:n.2384-223A>C
XR_937153.1:n.2309A>C
XR_937154.1:n.2309A>C
XR_937155.1:n.2230A>C
XR_937157.1:n.2232A>C
NM_001282447.2:c.2285A>C NP_001269376.1:p.His762Pro
NM_025220.4:c.2285A>C NP_079496.1:p.His762Pro
NM_153202.3:c.2207A>C NP_694882.1:p.His736Pro
XM_011529373.2:c.1322A>C XP_011527675.1:p.His441Pro
XR_001754405.1:n.2396A>C
XR_002958534.1:n.2505A>C
NM_001282447.3:c.2285A>C NP_001269376.1:p.His762Pro
NM_025220.5:c.2285A>C MANE Select NP_079496.1:p.His762Pro
NM_153202.4:c.2207A>C NP_694882.1:p.His736Pro