Canonical Allele Identifier: CA920153802
Gene: ADAM33 HGNC NCBI

Linked Data

dbSNP Id: rs1555832529

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3668986delinsGATCTG , CM000682.2:g.3668986delinsGATCTG GRCh38
NC_000020.10:g.3649633delinsGATCTG , CM000682.1:g.3649633delinsGATCTG GRCh37
NC_000020.9:g.3597633delinsGATCTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356518.7:c.2419delinsCAGATC MANE Select ENSP00000348912.3:p.Met807GlnfsTer12
ENST00000350009.6:c.2341delinsCAGATC ENSP00000322550.5:p.Met781GlnfsTer12
ENST00000356518.6:c.2419delinsCAGATC ENSP00000348912.2:p.Met807GlnfsTer12
ENST00000379861.8:c.2416delinsCAGATC ENSP00000369190.4:p.Met806GlnfsTer12
ENST00000466620.5:n.1980delinsCAGATC
ENST00000483362.1:n.1342delinsCAGATC
ENST00000617732.1:c.*1103delinsCAGATC ENSP00000483343.1:n.*1103delinsCAGATC
ENST00000619289.4:c.2056delinsCAGATC ENSP00000484600.1:p.Met686GlnfsTer12
NM_001282447.1:c.2416delinsCAGATC NP_001269376.1:p.Met806GlnfsTer12
NM_025220.3:c.2419delinsCAGATC NP_079496.1:p.Met807GlnfsTer12
NM_153202.2:c.2341delinsCAGATC NP_694882.1:p.Met781GlnfsTer12
XM_005260843.1:c.2458delinsCAGATC XP_005260900.1:p.Met820GlnfsTer12
XM_006723639.1:c.2455delinsCAGATC XP_006723702.1:p.Met819GlnfsTer12
XM_006723640.1:c.2449delinsCAGATC XP_006723703.1:p.Met817GlnfsTer12
XM_011529366.1:c.2455delinsCAGATC XP_011527668.1:p.Met819GlnfsTer12
XM_011529367.1:c.2416delinsCAGATC XP_011527669.1:p.Met806GlnfsTer12
XM_011529368.1:c.2380delinsCAGATC XP_011527670.1:p.Met794GlnfsTer12
XM_011529373.1:c.1456delinsCAGATC XP_011527675.1:p.Met486GlnfsTer12
XR_937151.1:n.2470delinsCAGATC
XR_937152.1:n.2467delinsCAGATC
XR_937153.1:n.2440delinsCAGATC
XR_937154.1:n.2440delinsCAGATC
XR_937155.1:n.2361delinsCAGATC
XR_937157.1:n.2363delinsCAGATC
NM_001282447.2:c.2416delinsCAGATC NP_001269376.1:p.Met806GlnfsTer12
NM_025220.4:c.2419delinsCAGATC NP_079496.1:p.Met807GlnfsTer12
NM_153202.3:c.2341delinsCAGATC NP_694882.1:p.Met781GlnfsTer12
XM_011529373.2:c.1456delinsCAGATC XP_011527675.1:p.Met486GlnfsTer12
XR_001754405.1:n.2527delinsCAGATC
XR_002958534.1:n.2636delinsCAGATC
NM_001282447.3:c.2416delinsCAGATC NP_001269376.1:p.Met806GlnfsTer12
NM_025220.5:c.2419delinsCAGATC MANE Select NP_079496.1:p.Met807GlnfsTer12
NM_153202.4:c.2341delinsCAGATC NP_694882.1:p.Met781GlnfsTer12