Canonical Allele Identifier: CA2651723738

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3669176-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669179del , CM000682.2:g.3669179del	GRCh38
NC_000020.10:g.3649826del , CM000682.1:g.3649826del	GRCh37
NC_000020.9:g.3597826del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2404+122del MANE Select	ENSP00000348912.3:n.2404+122del
ENST00000350009.6:c.2326+122del	ENSP00000322550.5:n.2326+122del
ENST00000356518.6:c.2404+122del	ENSP00000348912.2:n.2404+122del
ENST00000379861.8:c.2404+122del	ENSP00000369190.4:n.2404+122del
ENST00000466620.5:n.1965+122del
ENST00000483362.1:n.1327+122del
ENST00000617732.1:c.*1091+122del	ENSP00000483343.1:n.*1091+122del
ENST00000619289.4:c.2044+122del	ENSP00000484600.1:n.2044+122del
NM_001282447.1:c.2404+122del	NP_001269376.1:n.2404+122del
NM_025220.3:c.2404+122del	NP_079496.1:n.2404+122del
NM_153202.2:c.2326+122del	NP_694882.1:n.2326+122del
XM_005260843.1:c.2443+122del	XP_005260900.1:n.2443+122del
XM_006723639.1:c.2443+122del	XP_006723702.1:n.2443+122del
XM_006723640.1:c.2434+122del	XP_006723703.1:n.2434+122del
XM_011529366.1:c.2440+122del	XP_011527668.1:n.2440+122del
XM_011529367.1:c.2401+122del	XP_011527669.1:n.2401+122del
XM_011529368.1:c.2365+122del	XP_011527670.1:n.2365+122del
XM_011529373.1:c.1441+122del	XP_011527675.1:n.1441+122del
XR_937151.1:n.2455+122del
XR_937152.1:n.2455+122del
XR_937153.1:n.2428+122del
XR_937154.1:n.2428+122del
XR_937155.1:n.2349+122del
XR_937157.1:n.2351+122del
NM_001282447.2:c.2404+122del	NP_001269376.1:n.2404+122del
NM_025220.4:c.2404+122del	NP_079496.1:n.2404+122del
NM_153202.3:c.2326+122del	NP_694882.1:n.2326+122del
XM_011529373.2:c.1441+122del	XP_011527675.1:n.1441+122del
XR_001754405.1:n.2515+122del
XR_002958534.1:n.2624+122del
NM_001282447.3:c.2404+122del	NP_001269376.1:n.2404+122del
NM_025220.5:c.2404+122del MANE Select	NP_079496.1:n.2404+122del
NM_153202.4:c.2326+122del	NP_694882.1:n.2326+122del