Canonical Allele Identifier: CA2651723290
Gene: ADAM33 HGNC NCBI

Linked Data

gnomAD v4: 20-3668698-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3668698G>T , CM000682.2:g.3668698G>T GRCh38
NC_000020.10:g.3649345G>T , CM000682.1:g.3649345G>T GRCh37
NC_000020.9:g.3597345G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.*265C>A MANE Select ENSP00000348912.3:n.*265C>A
ENST00000350009.6:c.*265C>A ENSP00000322550.5:n.*265C>A
ENST00000356518.6:c.*265C>A ENSP00000348912.2:n.*265C>A
ENST00000379861.8:c.*265C>A ENSP00000369190.4:n.*265C>A
ENST00000466620.5:n.2268C>A
ENST00000483362.1:n.1630C>A
ENST00000617732.1:c.*1391C>A ENSP00000483343.1:n.*1391C>A
ENST00000619289.4:c.*265C>A ENSP00000484600.1:n.*265C>A
NM_001282447.1:c.*265C>A NP_001269376.1:n.*265C>A
NM_025220.3:c.*265C>A NP_079496.1:n.*265C>A
NM_153202.2:c.*265C>A NP_694882.1:n.*265C>A
XM_005260843.1:c.*265C>A XP_005260900.1:n.*265C>A
XM_006723639.1:c.*265C>A XP_006723702.1:n.*265C>A
XM_006723640.1:c.*265C>A XP_006723703.1:n.*265C>A
XM_011529366.1:c.*265C>A XP_011527668.1:n.*265C>A
XM_011529367.1:c.*265C>A XP_011527669.1:n.*265C>A
XM_011529368.1:c.*265C>A XP_011527670.1:n.*265C>A
XM_011529373.1:c.*265C>A XP_011527675.1:n.*265C>A
XR_937153.1:n.2728C>A
XR_937154.1:n.2728C>A
XR_937155.1:n.2649C>A
XR_937157.1:n.2651C>A
NM_001282447.2:c.*265C>A NP_001269376.1:n.*265C>A
NM_025220.4:c.*265C>A NP_079496.1:n.*265C>A
NM_153202.3:c.*265C>A NP_694882.1:n.*265C>A
XM_011529373.2:c.*265C>A XP_011527675.1:n.*265C>A
XR_001754405.1:n.2815C>A
XR_002958534.1:n.2924C>A
NM_001282447.3:c.*265C>A NP_001269376.1:n.*265C>A
NM_025220.5:c.*265C>A MANE Select NP_079496.1:n.*265C>A
NM_153202.4:c.*265C>A NP_694882.1:n.*265C>A