Canonical Allele Identifier: CA408105266

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652525T>C (hg19) ; chr20:g.3671878T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671878T>C , CM000682.2:g.3671878T>C	GRCh38
NC_000020.10:g.3652525T>C , CM000682.1:g.3652525T>C	GRCh37
NC_000020.9:g.3600525T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1705A>G MANE Select	ENSP00000348912.3:p.Arg569Gly
ENST00000350009.6:c.1705A>G	ENSP00000322550.5:p.Arg569Gly
ENST00000356518.6:c.1705A>G	ENSP00000348912.2:p.Arg569Gly
ENST00000379861.8:c.1705A>G	ENSP00000369190.4:p.Arg569Gly
ENST00000466620.5:n.1344A>G
ENST00000617732.1:c.*632-421A>G	ENSP00000483343.1:n.*632-421A>G
ENST00000619289.4:c.1345A>G	ENSP00000484600.1:p.Arg449Gly
NM_001282447.1:c.1705A>G	NP_001269376.1:p.Arg569Gly
NM_025220.3:c.1705A>G	NP_079496.1:p.Arg569Gly
NM_153202.2:c.1705A>G	NP_694882.1:p.Arg569Gly
XM_005260843.1:c.1744A>G	XP_005260900.1:p.Arg582Gly
XM_006723639.1:c.1744A>G	XP_006723702.1:p.Arg582Gly
XM_006723640.1:c.1735A>G	XP_006723703.1:p.Arg579Gly
XM_011529366.1:c.1741A>G	XP_011527668.1:p.Arg581Gly
XM_011529367.1:c.1702A>G	XP_011527669.1:p.Arg568Gly
XM_011529368.1:c.1744A>G	XP_011527670.1:p.Arg582Gly
XM_011529369.1:c.1712A>G	XP_011527671.1:p.Glu571Gly
XM_011529370.1:c.1712A>G	XP_011527672.1:p.Glu571Gly
XM_011529373.1:c.742A>G	XP_011527675.1:p.Arg248Gly
XR_937151.1:n.1848A>G
XR_937152.1:n.1848A>G
XR_937153.1:n.1729A>G
XR_937154.1:n.1729A>G
XR_937155.1:n.1650A>G
XR_937157.1:n.1652A>G
NM_001282447.2:c.1705A>G	NP_001269376.1:p.Arg569Gly
NM_025220.4:c.1705A>G	NP_079496.1:p.Arg569Gly
NM_153202.3:c.1705A>G	NP_694882.1:p.Arg569Gly
XM_011529373.2:c.742A>G	XP_011527675.1:p.Arg248Gly
XR_001754405.1:n.1816A>G
XR_002958534.1:n.1925A>G
NM_001282447.3:c.1705A>G	NP_001269376.1:p.Arg569Gly
NM_025220.5:c.1705A>G MANE Select	NP_079496.1:p.Arg569Gly
NM_153202.4:c.1705A>G	NP_694882.1:p.Arg569Gly