Canonical Allele Identifier: CA2651722743

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3668405-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668408del , CM000682.2:g.3668408del	GRCh38
NC_000020.10:g.3649055del , CM000682.1:g.3649055del	GRCh37
NC_000020.9:g.3597055del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.*557del MANE Select	ENSP00000348912.3:n.*557del
ENST00000350009.6:c.*557del	ENSP00000322550.5:n.*557del
ENST00000356518.6:c.*557del	ENSP00000348912.2:n.*557del
ENST00000379861.8:c.*557del	ENSP00000369190.4:n.*557del
ENST00000466620.5:n.2560del
ENST00000483362.1:n.1922del
ENST00000619289.4:c.*557del	ENSP00000484600.1:n.*557del
NM_001282447.1:c.*557del	NP_001269376.1:n.*557del
NM_025220.3:c.*557del	NP_079496.1:n.*557del
NM_153202.2:c.*557del	NP_694882.1:n.*557del
XM_005260843.1:c.*557del	XP_005260900.1:n.*557del
XM_006723639.1:c.*557del	XP_006723702.1:n.*557del
XM_006723640.1:c.*557del	XP_006723703.1:n.*557del
XM_011529366.1:c.*557del	XP_011527668.1:n.*557del
XM_011529367.1:c.*557del	XP_011527669.1:n.*557del
XM_011529368.1:c.*557del	XP_011527670.1:n.*557del
XM_011529373.1:c.*557del	XP_011527675.1:n.*557del
XR_937153.1:n.3020del
XR_937154.1:n.3020del
XR_937155.1:n.2941del
XR_937157.1:n.2943del
NM_001282447.2:c.*557del	NP_001269376.1:n.*557del
NM_025220.4:c.*557del	NP_079496.1:n.*557del
NM_153202.3:c.*557del	NP_694882.1:n.*557del
XM_011529373.2:c.*557del	XP_011527675.1:n.*557del
XR_001754405.1:n.3107del
XR_002958534.1:n.3216del
NM_001282447.3:c.*557del	NP_001269376.1:n.*557del
NM_025220.5:c.*557del MANE Select	NP_079496.1:n.*557del
NM_153202.4:c.*557del	NP_694882.1:n.*557del