Canonical Allele Identifier: CA509419216
Gene: ADAM33 HGNC NCBI

Linked Data

dbSNP Id: rs2087377979
MyVariant Identifiers: chr20:g.3650010C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669363C>T , CM000682.2:g.3669363C>T GRCh38
NC_000020.10:g.3650010C>T , CM000682.1:g.3650010C>T GRCh37
NC_000020.9:g.3598010C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356518.7:c.2340G>A MANE Select ENSP00000348912.3:p.Glu780=
ENST00000350009.6:c.2262G>A ENSP00000322550.5:p.Glu754=
ENST00000356518.6:c.2340G>A ENSP00000348912.2:p.Glu780=
ENST00000379861.8:c.2340G>A ENSP00000369190.4:p.Glu780=
ENST00000466620.5:n.1901G>A
ENST00000483362.1:n.1263G>A
ENST00000617732.1:c.*1027G>A ENSP00000483343.1:n.*1027G>A
ENST00000619289.4:c.1980G>A ENSP00000484600.1:p.Glu660=
NM_001282447.1:c.2340G>A NP_001269376.1:p.Glu780=
NM_025220.3:c.2340G>A NP_079496.1:p.Glu780=
NM_153202.2:c.2262G>A NP_694882.1:p.Glu754=
XM_005260843.1:c.2379G>A XP_005260900.1:p.Glu793=
XM_006723639.1:c.2379G>A XP_006723702.1:p.Glu793=
XM_006723640.1:c.2370G>A XP_006723703.1:p.Glu790=
XM_011529366.1:c.2376G>A XP_011527668.1:p.Glu792=
XM_011529367.1:c.2337G>A XP_011527669.1:p.Glu779=
XM_011529368.1:c.2301G>A XP_011527670.1:p.Glu767=
XM_011529373.1:c.1377G>A XP_011527675.1:p.Glu459=
XR_937151.1:n.2391G>A
XR_937152.1:n.2391G>A
XR_937153.1:n.2364G>A
XR_937154.1:n.2364G>A
XR_937155.1:n.2285G>A
XR_937157.1:n.2287G>A
NM_001282447.2:c.2340G>A NP_001269376.1:p.Glu780=
NM_025220.4:c.2340G>A NP_079496.1:p.Glu780=
NM_153202.3:c.2262G>A NP_694882.1:p.Glu754=
XM_011529373.2:c.1377G>A XP_011527675.1:p.Glu459=
XR_001754405.1:n.2451G>A
XR_002958534.1:n.2560G>A
NM_001282447.3:c.2340G>A NP_001269376.1:p.Glu780=
NM_025220.5:c.2340G>A MANE Select NP_079496.1:p.Glu780=
NM_153202.4:c.2262G>A NP_694882.1:p.Glu754=