Canonical Allele Identifier: CA2651724026

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3669633-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669637del , CM000682.2:g.3669637del	GRCh38
NC_000020.10:g.3650284del , CM000682.1:g.3650284del	GRCh37
NC_000020.9:g.3598284del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2244del MANE Select	ENSP00000348912.3:p.Asp750MetfsTer?
ENST00000350009.6:c.2166del	ENSP00000322550.5:p.Asp724MetfsTer?
ENST00000356518.6:c.2244del	ENSP00000348912.2:p.Asp750MetfsTer?
ENST00000379861.8:c.2244del	ENSP00000369190.4:p.Asp750MetfsTer?
ENST00000466620.5:n.1805del
ENST00000483362.1:n.992del
ENST00000617732.1:c.*931del	ENSP00000483343.1:n.*931del
ENST00000619289.4:c.1884del	ENSP00000484600.1:p.Asp630MetfsTer?
NM_001282447.1:c.2244del	NP_001269376.1:p.Asp750MetfsTer?
NM_025220.3:c.2244del	NP_079496.1:p.Asp750MetfsTer?
NM_153202.2:c.2166del	NP_694882.1:p.Asp724MetfsTer?
XM_005260843.1:c.2283del	XP_005260900.1:p.Asp763MetfsTer?
XM_006723639.1:c.2283del	XP_006723702.1:p.Asp763MetfsTer?
XM_006723640.1:c.2274del	XP_006723703.1:p.Asp760MetfsTer?
XM_011529366.1:c.2280del	XP_011527668.1:p.Asp762MetfsTer?
XM_011529367.1:c.2241del	XP_011527669.1:p.Asp749MetfsTer?
XM_011529368.1:c.2205del	XP_011527670.1:p.Asp737MetfsTer?
XM_011529373.1:c.1281del	XP_011527675.1:p.Asp429MetfsTer?
XR_937151.1:n.2384-264del
XR_937152.1:n.2384-264del
XR_937153.1:n.2268del
XR_937154.1:n.2268del
XR_937155.1:n.2189del
XR_937157.1:n.2191del
NM_001282447.2:c.2244del	NP_001269376.1:p.Asp750MetfsTer?
NM_025220.4:c.2244del	NP_079496.1:p.Asp750MetfsTer?
NM_153202.3:c.2166del	NP_694882.1:p.Asp724MetfsTer?
XM_011529373.2:c.1281del	XP_011527675.1:p.Asp429MetfsTer?
XR_001754405.1:n.2355del
XR_002958534.1:n.2464del
NM_001282447.3:c.2244del	NP_001269376.1:p.Asp750MetfsTer?
NM_025220.5:c.2244del MANE Select	NP_079496.1:p.Asp750MetfsTer?
NM_153202.4:c.2166del	NP_694882.1:p.Asp724MetfsTer?