Canonical Allele Identifier: CA509559766

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652066C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671419C>G , CM000682.2:g.3671419C>G	GRCh38
NC_000020.10:g.3652066C>G , CM000682.1:g.3652066C>G	GRCh37
NC_000020.9:g.3600066C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1983G>C MANE Select	ENSP00000348912.3:p.Gly661=
ENST00000350009.6:c.1906-74G>C	ENSP00000322550.5:n.1906-74G>C
ENST00000356518.6:c.1983G>C	ENSP00000348912.2:p.Gly661=
ENST00000379861.8:c.1983G>C	ENSP00000369190.4:p.Gly661=
ENST00000466620.5:n.1545-74G>C
ENST00000617732.1:c.*670G>C	ENSP00000483343.1:n.*670G>C
ENST00000619289.4:c.1623G>C	ENSP00000484600.1:p.Gly541=
NM_001282447.1:c.1983G>C	NP_001269376.1:p.Gly661=
NM_025220.3:c.1983G>C	NP_079496.1:p.Gly661=
NM_153202.2:c.1906-74G>C	NP_694882.1:n.1906-74G>C
XM_005260843.1:c.2022G>C	XP_005260900.1:p.Gly674=
XM_006723639.1:c.2022G>C	XP_006723702.1:p.Gly674=
XM_006723640.1:c.2013G>C	XP_006723703.1:p.Gly671=
XM_011529366.1:c.2019G>C	XP_011527668.1:p.Gly673=
XM_011529367.1:c.1980G>C	XP_011527669.1:p.Gly660=
XM_011529368.1:c.1945-74G>C	XP_011527670.1:n.1945-74G>C
XM_011529369.1:c.*82G>C	XP_011527671.1:n.*82G>C
XM_011529370.1:c.*5-74G>C	XP_011527672.1:n.*5-74G>C
XM_011529373.1:c.1020G>C	XP_011527675.1:p.Gly340=
XR_937151.1:n.2126G>C
XR_937152.1:n.2126G>C
XR_937153.1:n.2007G>C
XR_937154.1:n.2007G>C
XR_937155.1:n.1928G>C
XR_937157.1:n.1930G>C
NM_001282447.2:c.1983G>C	NP_001269376.1:p.Gly661=
NM_025220.4:c.1983G>C	NP_079496.1:p.Gly661=
NM_153202.3:c.1906-74G>C	NP_694882.1:n.1906-74G>C
XM_011529373.2:c.1020G>C	XP_011527675.1:p.Gly340=
XR_001754405.1:n.2094G>C
XR_002958534.1:n.2203G>C
NM_001282447.3:c.1983G>C	NP_001269376.1:p.Gly661=
NM_025220.5:c.1983G>C MANE Select	NP_079496.1:p.Gly661=
NM_153202.4:c.1906-74G>C	NP_694882.1:n.1906-74G>C