Canonical Allele Identifier: CA509419230

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3650209T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669562T>C , CM000682.2:g.3669562T>C	GRCh38
NC_000020.10:g.3650209T>C , CM000682.1:g.3650209T>C	GRCh37
NC_000020.9:g.3598209T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2316A>G MANE Select	ENSP00000348912.3:p.Gly772=
ENST00000350009.6:c.2238A>G	ENSP00000322550.5:p.Gly746=
ENST00000356518.6:c.2316A>G	ENSP00000348912.2:p.Gly772=
ENST00000379861.8:c.2316A>G	ENSP00000369190.4:p.Gly772=
ENST00000466620.5:n.1877A>G
ENST00000483362.1:n.1064A>G
ENST00000617732.1:c.*1003A>G	ENSP00000483343.1:n.*1003A>G
ENST00000619289.4:c.1956A>G	ENSP00000484600.1:p.Gly652=
NM_001282447.1:c.2316A>G	NP_001269376.1:p.Gly772=
NM_025220.3:c.2316A>G	NP_079496.1:p.Gly772=
NM_153202.2:c.2238A>G	NP_694882.1:p.Gly746=
XM_005260843.1:c.2355A>G	XP_005260900.1:p.Gly785=
XM_006723639.1:c.2355A>G	XP_006723702.1:p.Gly785=
XM_006723640.1:c.2346A>G	XP_006723703.1:p.Gly782=
XM_011529366.1:c.2352A>G	XP_011527668.1:p.Gly784=
XM_011529367.1:c.2313A>G	XP_011527669.1:p.Gly771=
XM_011529368.1:c.2277A>G	XP_011527670.1:p.Gly759=
XM_011529373.1:c.1353A>G	XP_011527675.1:p.Gly451=
XR_937151.1:n.2384-192A>G
XR_937152.1:n.2384-192A>G
XR_937153.1:n.2340A>G
XR_937154.1:n.2340A>G
XR_937155.1:n.2261A>G
XR_937157.1:n.2263A>G
NM_001282447.2:c.2316A>G	NP_001269376.1:p.Gly772=
NM_025220.4:c.2316A>G	NP_079496.1:p.Gly772=
NM_153202.3:c.2238A>G	NP_694882.1:p.Gly746=
XM_011529373.2:c.1353A>G	XP_011527675.1:p.Gly451=
XR_001754405.1:n.2427A>G
XR_002958534.1:n.2536A>G
NM_001282447.3:c.2316A>G	NP_001269376.1:p.Gly772=
NM_025220.5:c.2316A>G MANE Select	NP_079496.1:p.Gly772=
NM_153202.4:c.2238A>G	NP_694882.1:p.Gly746=