Canonical Allele Identifier: CA509419268

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3650269T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669622T>A , CM000682.2:g.3669622T>A	GRCh38
NC_000020.10:g.3650269T>A , CM000682.1:g.3650269T>A	GRCh37
NC_000020.9:g.3598269T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2256A>T MANE Select	ENSP00000348912.3:p.Pro752=
ENST00000350009.6:c.2178A>T	ENSP00000322550.5:p.Pro726=
ENST00000356518.6:c.2256A>T	ENSP00000348912.2:p.Pro752=
ENST00000379861.8:c.2256A>T	ENSP00000369190.4:p.Pro752=
ENST00000466620.5:n.1817A>T
ENST00000483362.1:n.1004A>T
ENST00000617732.1:c.*943A>T	ENSP00000483343.1:n.*943A>T
ENST00000619289.4:c.1896A>T	ENSP00000484600.1:p.Pro632=
NM_001282447.1:c.2256A>T	NP_001269376.1:p.Pro752=
NM_025220.3:c.2256A>T	NP_079496.1:p.Pro752=
NM_153202.2:c.2178A>T	NP_694882.1:p.Pro726=
XM_005260843.1:c.2295A>T	XP_005260900.1:p.Pro765=
XM_006723639.1:c.2295A>T	XP_006723702.1:p.Pro765=
XM_006723640.1:c.2286A>T	XP_006723703.1:p.Pro762=
XM_011529366.1:c.2292A>T	XP_011527668.1:p.Pro764=
XM_011529367.1:c.2253A>T	XP_011527669.1:p.Pro751=
XM_011529368.1:c.2217A>T	XP_011527670.1:p.Pro739=
XM_011529373.1:c.1293A>T	XP_011527675.1:p.Pro431=
XR_937151.1:n.2384-252A>T
XR_937152.1:n.2384-252A>T
XR_937153.1:n.2280A>T
XR_937154.1:n.2280A>T
XR_937155.1:n.2201A>T
XR_937157.1:n.2203A>T
NM_001282447.2:c.2256A>T	NP_001269376.1:p.Pro752=
NM_025220.4:c.2256A>T	NP_079496.1:p.Pro752=
NM_153202.3:c.2178A>T	NP_694882.1:p.Pro726=
XM_011529373.2:c.1293A>T	XP_011527675.1:p.Pro431=
XR_001754405.1:n.2367A>T
XR_002958534.1:n.2476A>T
NM_001282447.3:c.2256A>T	NP_001269376.1:p.Pro752=
NM_025220.5:c.2256A>T MANE Select	NP_079496.1:p.Pro752=
NM_153202.4:c.2178A>T	NP_694882.1:p.Pro726=