Canonical Allele Identifier: CA408103755

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3669563-C-A
• MyVariant Identifiers: chr20:g.3650210C>A (hg19) ; chr20:g.3669563C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669563C>A , CM000682.2:g.3669563C>A	GRCh38
NC_000020.10:g.3650210C>A , CM000682.1:g.3650210C>A	GRCh37
NC_000020.9:g.3598210C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2315G>T MANE Select	ENSP00000348912.3:p.Gly772Val
ENST00000350009.6:c.2237G>T	ENSP00000322550.5:p.Gly746Val
ENST00000356518.6:c.2315G>T	ENSP00000348912.2:p.Gly772Val
ENST00000379861.8:c.2315G>T	ENSP00000369190.4:p.Gly772Val
ENST00000466620.5:n.1876G>T
ENST00000483362.1:n.1063G>T
ENST00000617732.1:c.*1002G>T	ENSP00000483343.1:n.*1002G>T
ENST00000619289.4:c.1955G>T	ENSP00000484600.1:p.Gly652Val
NM_001282447.1:c.2315G>T	NP_001269376.1:p.Gly772Val
NM_025220.3:c.2315G>T	NP_079496.1:p.Gly772Val
NM_153202.2:c.2237G>T	NP_694882.1:p.Gly746Val
XM_005260843.1:c.2354G>T	XP_005260900.1:p.Gly785Val
XM_006723639.1:c.2354G>T	XP_006723702.1:p.Gly785Val
XM_006723640.1:c.2345G>T	XP_006723703.1:p.Gly782Val
XM_011529366.1:c.2351G>T	XP_011527668.1:p.Gly784Val
XM_011529367.1:c.2312G>T	XP_011527669.1:p.Gly771Val
XM_011529368.1:c.2276G>T	XP_011527670.1:p.Gly759Val
XM_011529373.1:c.1352G>T	XP_011527675.1:p.Gly451Val
XR_937151.1:n.2384-193G>T
XR_937152.1:n.2384-193G>T
XR_937153.1:n.2339G>T
XR_937154.1:n.2339G>T
XR_937155.1:n.2260G>T
XR_937157.1:n.2262G>T
NM_001282447.2:c.2315G>T	NP_001269376.1:p.Gly772Val
NM_025220.4:c.2315G>T	NP_079496.1:p.Gly772Val
NM_153202.3:c.2237G>T	NP_694882.1:p.Gly746Val
XM_011529373.2:c.1352G>T	XP_011527675.1:p.Gly451Val
XR_001754405.1:n.2426G>T
XR_002958534.1:n.2535G>T
NM_001282447.3:c.2315G>T	NP_001269376.1:p.Gly772Val
NM_025220.5:c.2315G>T MANE Select	NP_079496.1:p.Gly772Val
NM_153202.4:c.2237G>T	NP_694882.1:p.Gly746Val