Canonical Allele Identifier: CA408103433
Gene: ADAM33 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3668979C>T , CM000682.2:g.3668979C>T GRCh38
NC_000020.10:g.3649626C>T , CM000682.1:g.3649626C>T GRCh37
NC_000020.9:g.3597626C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2426G>A MANE Select ENSP00000348912.3:p.Arg809Lys
ENST00000350009.6:c.2348G>A ENSP00000322550.5:p.Arg783Lys
ENST00000356518.6:c.2426G>A ENSP00000348912.2:p.Arg809Lys
ENST00000379861.8:c.2423G>A ENSP00000369190.4:p.Arg808Lys
ENST00000466620.5:n.1987G>A
ENST00000483362.1:n.1349G>A
ENST00000617732.1:c.*1110G>A ENSP00000483343.1:n.*1110G>A
ENST00000619289.4:c.2063G>A ENSP00000484600.1:p.Arg688Lys
NM_001282447.1:c.2423G>A NP_001269376.1:p.Arg808Lys
NM_025220.3:c.2426G>A NP_079496.1:p.Arg809Lys
NM_153202.2:c.2348G>A NP_694882.1:p.Arg783Lys
XM_005260843.1:c.2465G>A XP_005260900.1:p.Arg822Lys
XM_006723639.1:c.2462G>A XP_006723702.1:p.Arg821Lys
XM_006723640.1:c.2456G>A XP_006723703.1:p.Arg819Lys
XM_011529366.1:c.2462G>A XP_011527668.1:p.Arg821Lys
XM_011529367.1:c.2423G>A XP_011527669.1:p.Arg808Lys
XM_011529368.1:c.2387G>A XP_011527670.1:p.Arg796Lys
XM_011529373.1:c.1463G>A XP_011527675.1:p.Arg488Lys
XR_937151.1:n.2477G>A
XR_937152.1:n.2474G>A
XR_937153.1:n.2447G>A
XR_937154.1:n.2447G>A
XR_937155.1:n.2368G>A
XR_937157.1:n.2370G>A
NM_001282447.2:c.2423G>A NP_001269376.1:p.Arg808Lys
NM_025220.4:c.2426G>A NP_079496.1:p.Arg809Lys
NM_153202.3:c.2348G>A NP_694882.1:p.Arg783Lys
XM_011529373.2:c.1463G>A XP_011527675.1:p.Arg488Lys
XR_001754405.1:n.2534G>A
XR_002958534.1:n.2643G>A
NM_001282447.3:c.2423G>A NP_001269376.1:p.Arg808Lys
NM_025220.5:c.2426G>A MANE Select NP_079496.1:p.Arg809Lys
NM_153202.4:c.2348G>A NP_694882.1:p.Arg783Lys