Canonical Allele Identifier: CA509559989

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652330G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671683G>T , CM000682.2:g.3671683G>T	GRCh38
NC_000020.10:g.3652330G>T , CM000682.1:g.3652330G>T	GRCh37
NC_000020.9:g.3600330G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1803C>A MANE Select	ENSP00000348912.3:p.Gly601=
ENST00000350009.6:c.1803C>A	ENSP00000322550.5:p.Gly601=
ENST00000356518.6:c.1803C>A	ENSP00000348912.2:p.Gly601=
ENST00000379861.8:c.1803C>A	ENSP00000369190.4:p.Gly601=
ENST00000466620.5:n.1442C>A
ENST00000617732.1:c.*632-226C>A	ENSP00000483343.1:n.*632-226C>A
ENST00000619289.4:c.1443C>A	ENSP00000484600.1:p.Gly481=
NM_001282447.1:c.1803C>A	NP_001269376.1:p.Gly601=
NM_025220.3:c.1803C>A	NP_079496.1:p.Gly601=
NM_153202.2:c.1803C>A	NP_694882.1:p.Gly601=
XM_005260843.1:c.1842C>A	XP_005260900.1:p.Gly614=
XM_006723639.1:c.1842C>A	XP_006723702.1:p.Gly614=
XM_006723640.1:c.1833C>A	XP_006723703.1:p.Gly611=
XM_011529366.1:c.1839C>A	XP_011527668.1:p.Gly613=
XM_011529367.1:c.1800C>A	XP_011527669.1:p.Gly600=
XM_011529368.1:c.1842C>A	XP_011527670.1:p.Gly614=
XM_011529369.1:c.1810C>A	XP_011527671.1:p.Pro604Thr
XM_011529370.1:c.1810C>A	XP_011527672.1:p.Pro604Thr
XM_011529373.1:c.840C>A	XP_011527675.1:p.Gly280=
XR_937151.1:n.1946C>A
XR_937152.1:n.1946C>A
XR_937153.1:n.1827C>A
XR_937154.1:n.1827C>A
XR_937155.1:n.1748C>A
XR_937157.1:n.1750C>A
NM_001282447.2:c.1803C>A	NP_001269376.1:p.Gly601=
NM_025220.4:c.1803C>A	NP_079496.1:p.Gly601=
NM_153202.3:c.1803C>A	NP_694882.1:p.Gly601=
XM_011529373.2:c.840C>A	XP_011527675.1:p.Gly280=
XR_001754405.1:n.1914C>A
XR_002958534.1:n.2023C>A
NM_001282447.3:c.1803C>A	NP_001269376.1:p.Gly601=
NM_025220.5:c.1803C>A MANE Select	NP_079496.1:p.Gly601=
NM_153202.4:c.1803C>A	NP_694882.1:p.Gly601=