Canonical Allele Identifier: CA408103834

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3650249C>T (hg19) ; chr20:g.3669602C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669602C>T , CM000682.2:g.3669602C>T	GRCh38
NC_000020.10:g.3650249C>T , CM000682.1:g.3650249C>T	GRCh37
NC_000020.9:g.3598249C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2276G>A MANE Select	ENSP00000348912.3:p.Gly759Asp
ENST00000350009.6:c.2198G>A	ENSP00000322550.5:p.Gly733Asp
ENST00000356518.6:c.2276G>A	ENSP00000348912.2:p.Gly759Asp
ENST00000379861.8:c.2276G>A	ENSP00000369190.4:p.Gly759Asp
ENST00000466620.5:n.1837G>A
ENST00000483362.1:n.1024G>A
ENST00000617732.1:c.*963G>A	ENSP00000483343.1:n.*963G>A
ENST00000619289.4:c.1916G>A	ENSP00000484600.1:p.Gly639Asp
NM_001282447.1:c.2276G>A	NP_001269376.1:p.Gly759Asp
NM_025220.3:c.2276G>A	NP_079496.1:p.Gly759Asp
NM_153202.2:c.2198G>A	NP_694882.1:p.Gly733Asp
XM_005260843.1:c.2315G>A	XP_005260900.1:p.Gly772Asp
XM_006723639.1:c.2315G>A	XP_006723702.1:p.Gly772Asp
XM_006723640.1:c.2306G>A	XP_006723703.1:p.Gly769Asp
XM_011529366.1:c.2312G>A	XP_011527668.1:p.Gly771Asp
XM_011529367.1:c.2273G>A	XP_011527669.1:p.Gly758Asp
XM_011529368.1:c.2237G>A	XP_011527670.1:p.Gly746Asp
XM_011529373.1:c.1313G>A	XP_011527675.1:p.Gly438Asp
XR_937151.1:n.2384-232G>A
XR_937152.1:n.2384-232G>A
XR_937153.1:n.2300G>A
XR_937154.1:n.2300G>A
XR_937155.1:n.2221G>A
XR_937157.1:n.2223G>A
NM_001282447.2:c.2276G>A	NP_001269376.1:p.Gly759Asp
NM_025220.4:c.2276G>A	NP_079496.1:p.Gly759Asp
NM_153202.3:c.2198G>A	NP_694882.1:p.Gly733Asp
XM_011529373.2:c.1313G>A	XP_011527675.1:p.Gly438Asp
XR_001754405.1:n.2387G>A
XR_002958534.1:n.2496G>A
NM_001282447.3:c.2276G>A	NP_001269376.1:p.Gly759Asp
NM_025220.5:c.2276G>A MANE Select	NP_079496.1:p.Gly759Asp
NM_153202.4:c.2198G>A	NP_694882.1:p.Gly733Asp