Canonical Allele Identifier: CA408104782
Gene: ADAM33 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3671472T>A , CM000682.2:g.3671472T>A GRCh38
NC_000020.10:g.3652119T>A , CM000682.1:g.3652119T>A GRCh37
NC_000020.9:g.3600119T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.1930A>T MANE Select ENSP00000348912.3:p.Lys644Ter
ENST00000350009.6:c.1905+109A>T ENSP00000322550.5:n.1905+109A>T
ENST00000356518.6:c.1930A>T ENSP00000348912.2:p.Lys644Ter
ENST00000379861.8:c.1930A>T ENSP00000369190.4:p.Lys644Ter
ENST00000466620.5:n.1544+109A>T
ENST00000617732.1:c.*632-15A>T ENSP00000483343.1:n.*632-15A>T
ENST00000619289.4:c.1570A>T ENSP00000484600.1:p.Lys524Ter
NM_001282447.1:c.1930A>T NP_001269376.1:p.Lys644Ter
NM_025220.3:c.1930A>T NP_079496.1:p.Lys644Ter
NM_153202.2:c.1905+109A>T NP_694882.1:n.1905+109A>T
XM_005260843.1:c.1969A>T XP_005260900.1:p.Lys657Ter
XM_006723639.1:c.1969A>T XP_006723702.1:p.Lys657Ter
XM_006723640.1:c.1960A>T XP_006723703.1:p.Lys654Ter
XM_011529366.1:c.1966A>T XP_011527668.1:p.Lys656Ter
XM_011529367.1:c.1927A>T XP_011527669.1:p.Lys643Ter
XM_011529368.1:c.1944+109A>T XP_011527670.1:n.1944+109A>T
XM_011529369.1:c.*29A>T XP_011527671.1:n.*29A>T
XM_011529370.1:c.*4+109A>T XP_011527672.1:n.*4+109A>T
XM_011529373.1:c.967A>T XP_011527675.1:p.Lys323Ter
XR_937151.1:n.2073A>T
XR_937152.1:n.2073A>T
XR_937153.1:n.1954A>T
XR_937154.1:n.1954A>T
XR_937155.1:n.1875A>T
XR_937157.1:n.1877A>T
NM_001282447.2:c.1930A>T NP_001269376.1:p.Lys644Ter
NM_025220.4:c.1930A>T NP_079496.1:p.Lys644Ter
NM_153202.3:c.1905+109A>T NP_694882.1:n.1905+109A>T
XM_011529373.2:c.967A>T XP_011527675.1:p.Lys323Ter
XR_001754405.1:n.2041A>T
XR_002958534.1:n.2150A>T
NM_001282447.3:c.1930A>T NP_001269376.1:p.Lys644Ter
NM_025220.5:c.1930A>T MANE Select NP_079496.1:p.Lys644Ter
NM_153202.4:c.1905+109A>T NP_694882.1:n.1905+109A>T