Canonical Allele Identifier: CA2346677492

Gene: ADAM33

Linked Data

• dbSNP Id: rs2087363759

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669172del , CM000682.2:g.3669172del	GRCh38
NC_000020.10:g.3649819del , CM000682.1:g.3649819del	GRCh37
NC_000020.9:g.3597819del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2404+128del MANE Select	ENSP00000348912.3:n.2404+128del
ENST00000350009.6:c.2326+128del	ENSP00000322550.5:n.2326+128del
ENST00000356518.6:c.2404+128del	ENSP00000348912.2:n.2404+128del
ENST00000379861.8:c.2404+128del	ENSP00000369190.4:n.2404+128del
ENST00000466620.5:n.1965+128del
ENST00000483362.1:n.1327+128del
ENST00000617732.1:c.*1091+128del	ENSP00000483343.1:n.*1091+128del
ENST00000619289.4:c.2044+128del	ENSP00000484600.1:n.2044+128del
NM_001282447.1:c.2404+128del	NP_001269376.1:n.2404+128del
NM_025220.3:c.2404+128del	NP_079496.1:n.2404+128del
NM_153202.2:c.2326+128del	NP_694882.1:n.2326+128del
XM_005260843.1:c.2443+128del	XP_005260900.1:n.2443+128del
XM_006723639.1:c.2443+128del	XP_006723702.1:n.2443+128del
XM_006723640.1:c.2434+128del	XP_006723703.1:n.2434+128del
XM_011529366.1:c.2440+128del	XP_011527668.1:n.2440+128del
XM_011529367.1:c.2401+128del	XP_011527669.1:n.2401+128del
XM_011529368.1:c.2365+128del	XP_011527670.1:n.2365+128del
XM_011529373.1:c.1441+128del	XP_011527675.1:n.1441+128del
XR_937151.1:n.2455+128del
XR_937152.1:n.2455+128del
XR_937153.1:n.2428+128del
XR_937154.1:n.2428+128del
XR_937155.1:n.2349+128del
XR_937157.1:n.2351+128del
NM_001282447.2:c.2404+128del	NP_001269376.1:n.2404+128del
NM_025220.4:c.2404+128del	NP_079496.1:n.2404+128del
NM_153202.3:c.2326+128del	NP_694882.1:n.2326+128del
XM_011529373.2:c.1441+128del	XP_011527675.1:n.1441+128del
XR_001754405.1:n.2515+128del
XR_002958534.1:n.2624+128del
NM_001282447.3:c.2404+128del	NP_001269376.1:n.2404+128del
NM_025220.5:c.2404+128del MANE Select	NP_079496.1:n.2404+128del
NM_153202.4:c.2326+128del	NP_694882.1:n.2326+128del