Canonical Allele Identifier: CA2346677182

Gene: ADAM33

Linked Data

• dbSNP Id: rs2087336748
• gnomAD v4: 20-3668582-C-CCT

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668584_3668585dup , CM000682.2:g.3668584_3668585dup	GRCh38
NC_000020.10:g.3649231_3649232dup , CM000682.1:g.3649231_3649232dup	GRCh37
NC_000020.9:g.3597231_3597232dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.*379_*380dup MANE Select	ENSP00000348912.3:n.*379_*380dup
ENST00000350009.6:c.*379_*380dup	ENSP00000322550.5:n.*379_*380dup
ENST00000356518.6:c.*379_*380dup	ENSP00000348912.2:n.*379_*380dup
ENST00000379861.8:c.*379_*380dup	ENSP00000369190.4:n.*379_*380dup
ENST00000466620.5:n.2382_2383dup
ENST00000483362.1:n.1744_1745dup
ENST00000617732.1:c.*1505_*1506dup	ENSP00000483343.1:n.*1505_*1506dup
ENST00000619289.4:c.*379_*380dup	ENSP00000484600.1:n.*379_*380dup
NM_001282447.1:c.*379_*380dup	NP_001269376.1:n.*379_*380dup
NM_025220.3:c.*379_*380dup	NP_079496.1:n.*379_*380dup
NM_153202.2:c.*379_*380dup	NP_694882.1:n.*379_*380dup
XM_005260843.1:c.*379_*380dup	XP_005260900.1:n.*379_*380dup
XM_006723639.1:c.*379_*380dup	XP_006723702.1:n.*379_*380dup
XM_006723640.1:c.*379_*380dup	XP_006723703.1:n.*379_*380dup
XM_011529366.1:c.*379_*380dup	XP_011527668.1:n.*379_*380dup
XM_011529367.1:c.*379_*380dup	XP_011527669.1:n.*379_*380dup
XM_011529368.1:c.*379_*380dup	XP_011527670.1:n.*379_*380dup
XM_011529373.1:c.*379_*380dup	XP_011527675.1:n.*379_*380dup
XR_937153.1:n.2842_2843dup
XR_937154.1:n.2842_2843dup
XR_937155.1:n.2763_2764dup
XR_937157.1:n.2765_2766dup
NM_001282447.2:c.*379_*380dup	NP_001269376.1:n.*379_*380dup
NM_025220.4:c.*379_*380dup	NP_079496.1:n.*379_*380dup
NM_153202.3:c.*379_*380dup	NP_694882.1:n.*379_*380dup
XM_011529373.2:c.*379_*380dup	XP_011527675.1:n.*379_*380dup
XR_001754405.1:n.2929_2930dup
XR_002958534.1:n.3038_3039dup
NM_001282447.3:c.*379_*380dup	NP_001269376.1:n.*379_*380dup
NM_025220.5:c.*379_*380dup MANE Select	NP_079496.1:n.*379_*380dup
NM_153202.4:c.*379_*380dup	NP_694882.1:n.*379_*380dup