Canonical Allele Identifier: CA509560395

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3673840-G-C
• MyVariant Identifiers: chr20:g.3654487G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3673840G>C , CM000682.2:g.3673840G>C	GRCh38
NC_000020.10:g.3654487G>C , CM000682.1:g.3654487G>C	GRCh37
NC_000020.9:g.3602487G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.810C>G MANE Select	ENSP00000348912.3:p.Arg270=
ENST00000350009.6:c.810C>G	ENSP00000322550.5:p.Arg270=
ENST00000356518.6:c.810C>G	ENSP00000348912.2:p.Arg270=
ENST00000379861.8:c.810C>G	ENSP00000369190.4:p.Arg270=
ENST00000617732.1:c.*631+472C>G	ENSP00000483343.1:n.*631+472C>G
ENST00000619289.4:c.806+4C>G	ENSP00000484600.1:n.806+4C>G
NM_001282447.1:c.810C>G	NP_001269376.1:p.Arg270=
NM_025220.3:c.810C>G	NP_079496.1:p.Arg270=
NM_153202.2:c.810C>G	NP_694882.1:p.Arg270=
XM_005260843.1:c.849C>G	XP_005260900.1:p.Arg283=
XM_006723639.1:c.849C>G	XP_006723702.1:p.Arg283=
XM_006723640.1:c.849C>G	XP_006723703.1:p.Arg283=
XM_006723644.2:c.849C>G	XP_006723707.1:p.Arg283=
XM_011529366.1:c.846C>G	XP_011527668.1:p.Arg282=
XM_011529367.1:c.807C>G	XP_011527669.1:p.Arg269=
XM_011529368.1:c.849C>G	XP_011527670.1:p.Arg283=
XM_011529369.1:c.849C>G	XP_011527671.1:p.Arg283=
XM_011529370.1:c.849C>G	XP_011527672.1:p.Arg283=
XM_011529371.1:c.849C>G	XP_011527673.1:p.Arg283=
XM_011529372.1:c.849C>G	XP_011527674.1:p.Arg283=
XM_011529373.1:c.-231C>G	XP_011527675.1:n.-231C>G
XR_937151.1:n.953C>G
XR_937152.1:n.953C>G
XR_937153.1:n.953C>G
XR_937154.1:n.953C>G
XR_937155.1:n.874C>G
XR_937157.1:n.953C>G
NM_001282447.2:c.810C>G	NP_001269376.1:p.Arg270=
NM_025220.4:c.810C>G	NP_079496.1:p.Arg270=
NM_153202.3:c.810C>G	NP_694882.1:p.Arg270=
XM_011529371.2:c.849C>G	XP_011527673.1:p.Arg283=
XM_011529373.2:c.-231C>G	XP_011527675.1:n.-231C>G
XM_017028080.2:c.849C>G	XP_016883569.1:p.Arg283=
XM_017028081.2:c.810C>G	XP_016883570.1:p.Arg270=
XM_017028082.1:c.849C>G	XP_016883571.1:p.Arg283=
XM_017028083.1:c.849C>G	XP_016883572.1:p.Arg283=
XR_001754405.1:n.953C>G
XR_002958534.1:n.953C>G
NM_001282447.3:c.810C>G	NP_001269376.1:p.Arg270=
NM_025220.5:c.810C>G MANE Select	NP_079496.1:p.Arg270=
NM_153202.4:c.810C>G	NP_694882.1:p.Arg270=