Canonical Allele Identifier: CA9745005
Gene: ADAM33 HGNC NCBI

Linked Data

dbSNP Id: rs543749

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669032G>T , CM000682.2:g.3669032G>T GRCh38
NC_000020.10:g.3649679G>T , CM000682.1:g.3649679G>T GRCh37
NC_000020.9:g.3597679G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2405-32C>A MANE Select ENSP00000348912.3:p.=
ENST00000350009.6:c.2327-32C>A ENSP00000322550.5:p.=
ENST00000356518.6:c.2405-32C>A ENSP00000348912.2:p.=
ENST00000379861.8:c.2405-35C>A ENSP00000369190.4:p.=
ENST00000466620.5:n.1966-32C>A
ENST00000483362.1:n.1328-32C>A
ENST00000617732.1:c.*1092-35C>A ENSP00000483343.1:p.=
ENST00000619289.4:c.2045-35C>A ENSP00000484600.1:p.=
NM_001282447.1:c.2405-35C>A NP_001269376.1:p.=
NM_025220.3:c.2405-32C>A NP_079496.1:p.=
NM_153202.2:c.2327-32C>A NP_694882.1:p.=
XM_005260843.1:c.2444-32C>A XP_005260900.1:p.=
XM_006723639.1:c.2444-35C>A XP_006723702.1:p.=
XM_006723640.1:c.2435-32C>A XP_006723703.1:p.=
XM_011529366.1:c.2441-32C>A XP_011527668.1:p.=
XM_011529367.1:c.2402-32C>A XP_011527669.1:p.=
XM_011529368.1:c.2366-32C>A XP_011527670.1:p.=
XM_011529373.1:c.1442-32C>A XP_011527675.1:p.=
XR_937151.1:n.2456-32C>A
XR_937152.1:n.2456-35C>A
XR_937153.1:n.2429-35C>A
XR_937154.1:n.2429-35C>A
XR_937155.1:n.2350-35C>A
XR_937157.1:n.2352-35C>A
NM_001282447.2:c.2405-35C>A NP_001269376.1:p.=
NM_025220.4:c.2405-32C>A NP_079496.1:p.=
NM_153202.3:c.2327-32C>A NP_694882.1:p.=
XM_011529373.2:c.1442-32C>A XP_011527675.1:p.=
XR_001754405.1:n.2516-35C>A
XR_002958534.1:n.2625-35C>A
NM_001282447.3:c.2405-35C>A NP_001269376.1:p.=
NM_025220.5:c.2405-32C>A MANE Select NP_079496.1:p.=
NM_153202.4:c.2327-32C>A NP_694882.1:p.=