Canonical Allele Identifier: CA744017456

Gene: ADAM33

Linked Data

• dbSNP Id: rs1460029937
• gnomAD v3: 20-3673659-C-CT
• gnomAD v4: 20-3673659-C-CT
• MyVariant Identifiers: chr20:g.3654306_3654307insT (hg19) ; chr20:g.3673659_3673660insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3673660dup , CM000682.2:g.3673660dup	GRCh38
NC_000020.10:g.3654307dup , CM000682.1:g.3654307dup	GRCh37
NC_000020.9:g.3602307dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.906-2dup MANE Select	ENSP00000348912.3:n.906-2dup
ENST00000350009.6:c.906-2dup	ENSP00000322550.5:n.906-2dup
ENST00000356518.6:c.906-2dup	ENSP00000348912.2:n.906-2dup
ENST00000379861.8:c.906-2dup	ENSP00000369190.4:n.906-2dup
ENST00000466620.5:n.88dup
ENST00000617732.1:c.*631+652dup	ENSP00000483343.1:n.*631+652dup
ENST00000619289.4:c.806+184dup	ENSP00000484600.1:n.806+184dup
NM_001282447.1:c.906-2dup	NP_001269376.1:n.906-2dup
NM_025220.3:c.906-2dup	NP_079496.1:n.906-2dup
NM_153202.2:c.906-2dup	NP_694882.1:n.906-2dup
XM_005260843.1:c.945-2dup	XP_005260900.1:n.945-2dup
XM_006723639.1:c.945-2dup	XP_006723702.1:n.945-2dup
XM_006723640.1:c.945-2dup	XP_006723703.1:n.945-2dup
XM_006723644.2:c.945-2dup	XP_006723707.1:n.945-2dup
XM_011529366.1:c.942-2dup	XP_011527668.1:n.942-2dup
XM_011529367.1:c.903-2dup	XP_011527669.1:n.903-2dup
XM_011529368.1:c.945-2dup	XP_011527670.1:n.945-2dup
XM_011529369.1:c.945-2dup	XP_011527671.1:n.945-2dup
XM_011529370.1:c.945-2dup	XP_011527672.1:n.945-2dup
XM_011529371.1:c.945-2dup	XP_011527673.1:n.945-2dup
XM_011529372.1:c.945-2dup	XP_011527674.1:n.945-2dup
XM_011529373.1:c.-51dup	XP_011527675.1:n.-51dup
XR_937151.1:n.1049-2dup
XR_937152.1:n.1049-2dup
XR_937153.1:n.1049-2dup
XR_937154.1:n.1133dup
XR_937155.1:n.1054dup
XR_937157.1:n.1049-2dup
NM_001282447.2:c.906-2dup	NP_001269376.1:n.906-2dup
NM_025220.4:c.906-2dup	NP_079496.1:n.906-2dup
NM_153202.3:c.906-2dup	NP_694882.1:n.906-2dup
XM_011529371.2:c.945-2dup	XP_011527673.1:n.945-2dup
XM_011529373.2:c.-51dup	XP_011527675.1:n.-51dup
XM_017028080.2:c.1029dup	XP_016883569.1:p.Gly344ArgfsTer?
XM_017028081.2:c.990dup	XP_016883570.1:p.Gly331ArgfsTer?
XM_017028082.1:c.945-2dup	XP_016883571.1:n.945-2dup
XM_017028083.1:c.945-2dup	XP_016883572.1:n.945-2dup
XR_001754405.1:n.1049-2dup
XR_002958534.1:n.1049-2dup
NM_001282447.3:c.906-2dup	NP_001269376.1:n.906-2dup
NM_025220.5:c.906-2dup MANE Select	NP_079496.1:n.906-2dup
NM_153202.4:c.906-2dup	NP_694882.1:n.906-2dup