Canonical Allele Identifier: CA408103758

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3669564-C-T
• MyVariant Identifiers: chr20:g.3650211C>T (hg19) ; chr20:g.3669564C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669564C>T , CM000682.2:g.3669564C>T	GRCh38
NC_000020.10:g.3650211C>T , CM000682.1:g.3650211C>T	GRCh37
NC_000020.9:g.3598211C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2314G>A MANE Select	ENSP00000348912.3:p.Gly772Arg
ENST00000350009.6:c.2236G>A	ENSP00000322550.5:p.Gly746Arg
ENST00000356518.6:c.2314G>A	ENSP00000348912.2:p.Gly772Arg
ENST00000379861.8:c.2314G>A	ENSP00000369190.4:p.Gly772Arg
ENST00000466620.5:n.1875G>A
ENST00000483362.1:n.1062G>A
ENST00000617732.1:c.*1001G>A	ENSP00000483343.1:n.*1001G>A
ENST00000619289.4:c.1954G>A	ENSP00000484600.1:p.Gly652Arg
NM_001282447.1:c.2314G>A	NP_001269376.1:p.Gly772Arg
NM_025220.3:c.2314G>A	NP_079496.1:p.Gly772Arg
NM_153202.2:c.2236G>A	NP_694882.1:p.Gly746Arg
XM_005260843.1:c.2353G>A	XP_005260900.1:p.Gly785Arg
XM_006723639.1:c.2353G>A	XP_006723702.1:p.Gly785Arg
XM_006723640.1:c.2344G>A	XP_006723703.1:p.Gly782Arg
XM_011529366.1:c.2350G>A	XP_011527668.1:p.Gly784Arg
XM_011529367.1:c.2311G>A	XP_011527669.1:p.Gly771Arg
XM_011529368.1:c.2275G>A	XP_011527670.1:p.Gly759Arg
XM_011529373.1:c.1351G>A	XP_011527675.1:p.Gly451Arg
XR_937151.1:n.2384-194G>A
XR_937152.1:n.2384-194G>A
XR_937153.1:n.2338G>A
XR_937154.1:n.2338G>A
XR_937155.1:n.2259G>A
XR_937157.1:n.2261G>A
NM_001282447.2:c.2314G>A	NP_001269376.1:p.Gly772Arg
NM_025220.4:c.2314G>A	NP_079496.1:p.Gly772Arg
NM_153202.3:c.2236G>A	NP_694882.1:p.Gly746Arg
XM_011529373.2:c.1351G>A	XP_011527675.1:p.Gly451Arg
XR_001754405.1:n.2425G>A
XR_002958534.1:n.2534G>A
NM_001282447.3:c.2314G>A	NP_001269376.1:p.Gly772Arg
NM_025220.5:c.2314G>A MANE Select	NP_079496.1:p.Gly772Arg
NM_153202.4:c.2236G>A	NP_694882.1:p.Gly746Arg