Canonical Allele Identifier: CA408103800

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3650232C>G (hg19) ; chr20:g.3669585C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669585C>G , CM000682.2:g.3669585C>G	GRCh38
NC_000020.10:g.3650232C>G , CM000682.1:g.3650232C>G	GRCh37
NC_000020.9:g.3598232C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2293G>C MANE Select	ENSP00000348912.3:p.Glu765Gln
ENST00000350009.6:c.2215G>C	ENSP00000322550.5:p.Glu739Gln
ENST00000356518.6:c.2293G>C	ENSP00000348912.2:p.Glu765Gln
ENST00000379861.8:c.2293G>C	ENSP00000369190.4:p.Glu765Gln
ENST00000466620.5:n.1854G>C
ENST00000483362.1:n.1041G>C
ENST00000617732.1:c.*980G>C	ENSP00000483343.1:n.*980G>C
ENST00000619289.4:c.1933G>C	ENSP00000484600.1:p.Glu645Gln
NM_001282447.1:c.2293G>C	NP_001269376.1:p.Glu765Gln
NM_025220.3:c.2293G>C	NP_079496.1:p.Glu765Gln
NM_153202.2:c.2215G>C	NP_694882.1:p.Glu739Gln
XM_005260843.1:c.2332G>C	XP_005260900.1:p.Glu778Gln
XM_006723639.1:c.2332G>C	XP_006723702.1:p.Glu778Gln
XM_006723640.1:c.2323G>C	XP_006723703.1:p.Glu775Gln
XM_011529366.1:c.2329G>C	XP_011527668.1:p.Glu777Gln
XM_011529367.1:c.2290G>C	XP_011527669.1:p.Glu764Gln
XM_011529368.1:c.2254G>C	XP_011527670.1:p.Glu752Gln
XM_011529373.1:c.1330G>C	XP_011527675.1:p.Glu444Gln
XR_937151.1:n.2384-215G>C
XR_937152.1:n.2384-215G>C
XR_937153.1:n.2317G>C
XR_937154.1:n.2317G>C
XR_937155.1:n.2238G>C
XR_937157.1:n.2240G>C
NM_001282447.2:c.2293G>C	NP_001269376.1:p.Glu765Gln
NM_025220.4:c.2293G>C	NP_079496.1:p.Glu765Gln
NM_153202.3:c.2215G>C	NP_694882.1:p.Glu739Gln
XM_011529373.2:c.1330G>C	XP_011527675.1:p.Glu444Gln
XR_001754405.1:n.2404G>C
XR_002958534.1:n.2513G>C
NM_001282447.3:c.2293G>C	NP_001269376.1:p.Glu765Gln
NM_025220.5:c.2293G>C MANE Select	NP_079496.1:p.Glu765Gln
NM_153202.4:c.2215G>C	NP_694882.1:p.Glu739Gln