Canonical Allele Identifier: CA2651722307

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3667976-GTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3667978_3667979del , CM000682.2:g.3667978_3667979del	GRCh38
NC_000020.10:g.3648625_3648626del , CM000682.1:g.3648625_3648626del	GRCh37
NC_000020.9:g.3596625_3596626del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.*985_*986del MANE Select	ENSP00000348912.3:n.*985_*986del
ENST00000350009.6:c.*985_*986del	ENSP00000322550.5:n.*985_*986del
ENST00000356518.6:c.*985_*986del	ENSP00000348912.2:n.*985_*986del
ENST00000379861.8:c.*985_*986del	ENSP00000369190.4:n.*985_*986del
ENST00000466620.5:n.2988_2989del
ENST00000483362.1:n.2350_2351del
ENST00000619289.4:c.*985_*986del	ENSP00000484600.1:n.*985_*986del
NM_001282447.1:c.*985_*986del	NP_001269376.1:n.*985_*986del
NM_025220.3:c.*985_*986del	NP_079496.1:n.*985_*986del
NM_153202.2:c.*985_*986del	NP_694882.1:n.*985_*986del
XM_005260843.1:c.*985_*986del	XP_005260900.1:n.*985_*986del
XM_006723639.1:c.*985_*986del	XP_006723702.1:n.*985_*986del
XM_006723640.1:c.*985_*986del	XP_006723703.1:n.*985_*986del
XM_011529366.1:c.*985_*986del	XP_011527668.1:n.*985_*986del
XM_011529367.1:c.*985_*986del	XP_011527669.1:n.*985_*986del
XM_011529368.1:c.*985_*986del	XP_011527670.1:n.*985_*986del
XM_011529373.1:c.*985_*986del	XP_011527675.1:n.*985_*986del
XR_937153.1:n.3448_3449del
XR_937154.1:n.3448_3449del
XR_937155.1:n.3369_3370del
XR_937157.1:n.3371_3372del
NM_001282447.2:c.*985_*986del	NP_001269376.1:n.*985_*986del
NM_025220.4:c.*985_*986del	NP_079496.1:n.*985_*986del
NM_153202.3:c.*985_*986del	NP_694882.1:n.*985_*986del
XM_011529373.2:c.*985_*986del	XP_011527675.1:n.*985_*986del
XR_001754405.1:n.3535_3536del
XR_002958534.1:n.3644_3645del
NM_001282447.3:c.*985_*986del	NP_001269376.1:n.*985_*986del
NM_025220.5:c.*985_*986del MANE Select	NP_079496.1:n.*985_*986del
NM_153202.4:c.*985_*986del	NP_694882.1:n.*985_*986del