Canonical Allele Identifier: CA408103807
Gene: ADAM33 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2290A>T MANE Select ENSP00000348912.3:p.Met764Leu
ENST00000350009.6:c.2212A>T ENSP00000322550.5:p.Met738Leu
ENST00000356518.6:c.2290A>T ENSP00000348912.2:p.Met764Leu
ENST00000379861.8:c.2290A>T ENSP00000369190.4:p.Met764Leu
ENST00000466620.5:n.1851A>T
ENST00000483362.1:n.1038A>T
ENST00000617732.1:c.*977A>T ENSP00000483343.1:n.*977A>T
ENST00000619289.4:c.1930A>T ENSP00000484600.1:p.Met644Leu
NM_001282447.1:c.2290A>T NP_001269376.1:p.Met764Leu
NM_025220.3:c.2290A>T NP_079496.1:p.Met764Leu
NM_153202.2:c.2212A>T NP_694882.1:p.Met738Leu
XM_005260843.1:c.2329A>T XP_005260900.1:p.Met777Leu
XM_006723639.1:c.2329A>T XP_006723702.1:p.Met777Leu
XM_006723640.1:c.2320A>T XP_006723703.1:p.Met774Leu
XM_011529366.1:c.2326A>T XP_011527668.1:p.Met776Leu
XM_011529367.1:c.2287A>T XP_011527669.1:p.Met763Leu
XM_011529368.1:c.2251A>T XP_011527670.1:p.Met751Leu
XM_011529373.1:c.1327A>T XP_011527675.1:p.Met443Leu
XR_937151.1:n.2384-218A>T
XR_937152.1:n.2384-218A>T
XR_937153.1:n.2314A>T
XR_937154.1:n.2314A>T
XR_937155.1:n.2235A>T
XR_937157.1:n.2237A>T
NM_001282447.2:c.2290A>T NP_001269376.1:p.Met764Leu
NM_025220.4:c.2290A>T NP_079496.1:p.Met764Leu
NM_153202.3:c.2212A>T NP_694882.1:p.Met738Leu
XM_011529373.2:c.1327A>T XP_011527675.1:p.Met443Leu
XR_001754405.1:n.2401A>T
XR_002958534.1:n.2510A>T
NM_001282447.3:c.2290A>T NP_001269376.1:p.Met764Leu
NM_025220.5:c.2290A>T MANE Select NP_079496.1:p.Met764Leu
NM_153202.4:c.2212A>T NP_694882.1:p.Met738Leu