Canonical Allele Identifier: CA408103635

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3650005G>T (hg19) ; chr20:g.3669358G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669358G>T , CM000682.2:g.3669358G>T	GRCh38
NC_000020.10:g.3650005G>T , CM000682.1:g.3650005G>T	GRCh37
NC_000020.9:g.3598005G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2345C>A MANE Select	ENSP00000348912.3:p.Ser782Tyr
ENST00000350009.6:c.2267C>A	ENSP00000322550.5:p.Ser756Tyr
ENST00000356518.6:c.2345C>A	ENSP00000348912.2:p.Ser782Tyr
ENST00000379861.8:c.2345C>A	ENSP00000369190.4:p.Ser782Tyr
ENST00000466620.5:n.1906C>A
ENST00000483362.1:n.1268C>A
ENST00000617732.1:c.*1032C>A	ENSP00000483343.1:n.*1032C>A
ENST00000619289.4:c.1985C>A	ENSP00000484600.1:p.Ser662Tyr
NM_001282447.1:c.2345C>A	NP_001269376.1:p.Ser782Tyr
NM_025220.3:c.2345C>A	NP_079496.1:p.Ser782Tyr
NM_153202.2:c.2267C>A	NP_694882.1:p.Ser756Tyr
XM_005260843.1:c.2384C>A	XP_005260900.1:p.Ser795Tyr
XM_006723639.1:c.2384C>A	XP_006723702.1:p.Ser795Tyr
XM_006723640.1:c.2375C>A	XP_006723703.1:p.Ser792Tyr
XM_011529366.1:c.2381C>A	XP_011527668.1:p.Ser794Tyr
XM_011529367.1:c.2342C>A	XP_011527669.1:p.Ser781Tyr
XM_011529368.1:c.2306C>A	XP_011527670.1:p.Ser769Tyr
XM_011529373.1:c.1382C>A	XP_011527675.1:p.Ser461Tyr
XR_937151.1:n.2396C>A
XR_937152.1:n.2396C>A
XR_937153.1:n.2369C>A
XR_937154.1:n.2369C>A
XR_937155.1:n.2290C>A
XR_937157.1:n.2292C>A
NM_001282447.2:c.2345C>A	NP_001269376.1:p.Ser782Tyr
NM_025220.4:c.2345C>A	NP_079496.1:p.Ser782Tyr
NM_153202.3:c.2267C>A	NP_694882.1:p.Ser756Tyr
XM_011529373.2:c.1382C>A	XP_011527675.1:p.Ser461Tyr
XR_001754405.1:n.2456C>A
XR_002958534.1:n.2565C>A
NM_001282447.3:c.2345C>A	NP_001269376.1:p.Ser782Tyr
NM_025220.5:c.2345C>A MANE Select	NP_079496.1:p.Ser782Tyr
NM_153202.4:c.2267C>A	NP_694882.1:p.Ser756Tyr