Canonical Allele Identifier: CA408104927

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652265C>T (hg19) ; chr20:g.3671618C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671618C>T , CM000682.2:g.3671618C>T	GRCh38
NC_000020.10:g.3652265C>T , CM000682.1:g.3652265C>T	GRCh37
NC_000020.9:g.3600265C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1868G>A MANE Select	ENSP00000348912.3:p.Gly623Asp
ENST00000350009.6:c.1868G>A	ENSP00000322550.5:p.Gly623Asp
ENST00000356518.6:c.1868G>A	ENSP00000348912.2:p.Gly623Asp
ENST00000379861.8:c.1868G>A	ENSP00000369190.4:p.Gly623Asp
ENST00000466620.5:n.1507G>A
ENST00000617732.1:c.*632-161G>A	ENSP00000483343.1:n.*632-161G>A
ENST00000619289.4:c.1508G>A	ENSP00000484600.1:p.Gly503Asp
NM_001282447.1:c.1868G>A	NP_001269376.1:p.Gly623Asp
NM_025220.3:c.1868G>A	NP_079496.1:p.Gly623Asp
NM_153202.2:c.1868G>A	NP_694882.1:p.Gly623Asp
XM_005260843.1:c.1907G>A	XP_005260900.1:p.Gly636Asp
XM_006723639.1:c.1907G>A	XP_006723702.1:p.Gly636Asp
XM_006723640.1:c.1898G>A	XP_006723703.1:p.Gly633Asp
XM_011529366.1:c.1904G>A	XP_011527668.1:p.Gly635Asp
XM_011529367.1:c.1865G>A	XP_011527669.1:p.Gly622Asp
XM_011529368.1:c.1907G>A	XP_011527670.1:p.Gly636Asp
XM_011529369.1:c.1875G>A	XP_011527671.1:p.Gly625=
XM_011529370.1:c.1875G>A	XP_011527672.1:p.Gly625=
XM_011529373.1:c.905G>A	XP_011527675.1:p.Gly302Asp
XR_937151.1:n.2011G>A
XR_937152.1:n.2011G>A
XR_937153.1:n.1892G>A
XR_937154.1:n.1892G>A
XR_937155.1:n.1813G>A
XR_937157.1:n.1815G>A
NM_001282447.2:c.1868G>A	NP_001269376.1:p.Gly623Asp
NM_025220.4:c.1868G>A	NP_079496.1:p.Gly623Asp
NM_153202.3:c.1868G>A	NP_694882.1:p.Gly623Asp
XM_011529373.2:c.905G>A	XP_011527675.1:p.Gly302Asp
XR_001754405.1:n.1979G>A
XR_002958534.1:n.2088G>A
NM_001282447.3:c.1868G>A	NP_001269376.1:p.Gly623Asp
NM_025220.5:c.1868G>A MANE Select	NP_079496.1:p.Gly623Asp
NM_153202.4:c.1868G>A	NP_694882.1:p.Gly623Asp