Canonical Allele Identifier: CA408103653

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3650009T>A (hg19) ; chr20:g.3669362T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669362T>A , CM000682.2:g.3669362T>A	GRCh38
NC_000020.10:g.3650009T>A , CM000682.1:g.3650009T>A	GRCh37
NC_000020.9:g.3598009T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2341A>T MANE Select	ENSP00000348912.3:p.Asn781Tyr
ENST00000350009.6:c.2263A>T	ENSP00000322550.5:p.Asn755Tyr
ENST00000356518.6:c.2341A>T	ENSP00000348912.2:p.Asn781Tyr
ENST00000379861.8:c.2341A>T	ENSP00000369190.4:p.Asn781Tyr
ENST00000466620.5:n.1902A>T
ENST00000483362.1:n.1264A>T
ENST00000617732.1:c.*1028A>T	ENSP00000483343.1:n.*1028A>T
ENST00000619289.4:c.1981A>T	ENSP00000484600.1:p.Asn661Tyr
NM_001282447.1:c.2341A>T	NP_001269376.1:p.Asn781Tyr
NM_025220.3:c.2341A>T	NP_079496.1:p.Asn781Tyr
NM_153202.2:c.2263A>T	NP_694882.1:p.Asn755Tyr
XM_005260843.1:c.2380A>T	XP_005260900.1:p.Asn794Tyr
XM_006723639.1:c.2380A>T	XP_006723702.1:p.Asn794Tyr
XM_006723640.1:c.2371A>T	XP_006723703.1:p.Asn791Tyr
XM_011529366.1:c.2377A>T	XP_011527668.1:p.Asn793Tyr
XM_011529367.1:c.2338A>T	XP_011527669.1:p.Asn780Tyr
XM_011529368.1:c.2302A>T	XP_011527670.1:p.Asn768Tyr
XM_011529373.1:c.1378A>T	XP_011527675.1:p.Asn460Tyr
XR_937151.1:n.2392A>T
XR_937152.1:n.2392A>T
XR_937153.1:n.2365A>T
XR_937154.1:n.2365A>T
XR_937155.1:n.2286A>T
XR_937157.1:n.2288A>T
NM_001282447.2:c.2341A>T	NP_001269376.1:p.Asn781Tyr
NM_025220.4:c.2341A>T	NP_079496.1:p.Asn781Tyr
NM_153202.3:c.2263A>T	NP_694882.1:p.Asn755Tyr
XM_011529373.2:c.1378A>T	XP_011527675.1:p.Asn460Tyr
XR_001754405.1:n.2452A>T
XR_002958534.1:n.2561A>T
NM_001282447.3:c.2341A>T	NP_001269376.1:p.Asn781Tyr
NM_025220.5:c.2341A>T MANE Select	NP_079496.1:p.Asn781Tyr
NM_153202.4:c.2263A>T	NP_694882.1:p.Asn755Tyr