Canonical Allele Identifier: CA408104788

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652121C>G (hg19) ; chr20:g.3671474C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671474C>G , CM000682.2:g.3671474C>G	GRCh38
NC_000020.10:g.3652121C>G , CM000682.1:g.3652121C>G	GRCh37
NC_000020.9:g.3600121C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.1928G>C MANE Select	ENSP00000348912.3:p.Arg643Thr
ENST00000350009.6:c.1905+107G>C	ENSP00000322550.5:n.1905+107G>C
ENST00000356518.6:c.1928G>C	ENSP00000348912.2:p.Arg643Thr
ENST00000379861.8:c.1928G>C	ENSP00000369190.4:p.Arg643Thr
ENST00000466620.5:n.1544+107G>C
ENST00000617732.1:c.*632-17G>C	ENSP00000483343.1:n.*632-17G>C
ENST00000619289.4:c.1568G>C	ENSP00000484600.1:p.Arg523Thr
NM_001282447.1:c.1928G>C	NP_001269376.1:p.Arg643Thr
NM_025220.3:c.1928G>C	NP_079496.1:p.Arg643Thr
NM_153202.2:c.1905+107G>C	NP_694882.1:n.1905+107G>C
XM_005260843.1:c.1967G>C	XP_005260900.1:p.Arg656Thr
XM_006723639.1:c.1967G>C	XP_006723702.1:p.Arg656Thr
XM_006723640.1:c.1958G>C	XP_006723703.1:p.Arg653Thr
XM_011529366.1:c.1964G>C	XP_011527668.1:p.Arg655Thr
XM_011529367.1:c.1925G>C	XP_011527669.1:p.Arg642Thr
XM_011529368.1:c.1944+107G>C	XP_011527670.1:n.1944+107G>C
XM_011529369.1:c.*27G>C	XP_011527671.1:n.*27G>C
XM_011529370.1:c.*4+107G>C	XP_011527672.1:n.*4+107G>C
XM_011529373.1:c.965G>C	XP_011527675.1:p.Arg322Thr
XR_937151.1:n.2071G>C
XR_937152.1:n.2071G>C
XR_937153.1:n.1952G>C
XR_937154.1:n.1952G>C
XR_937155.1:n.1873G>C
XR_937157.1:n.1875G>C
NM_001282447.2:c.1928G>C	NP_001269376.1:p.Arg643Thr
NM_025220.4:c.1928G>C	NP_079496.1:p.Arg643Thr
NM_153202.3:c.1905+107G>C	NP_694882.1:n.1905+107G>C
XM_011529373.2:c.965G>C	XP_011527675.1:p.Arg322Thr
XR_001754405.1:n.2039G>C
XR_002958534.1:n.2148G>C
NM_001282447.3:c.1928G>C	NP_001269376.1:p.Arg643Thr
NM_025220.5:c.1928G>C MANE Select	NP_079496.1:p.Arg643Thr
NM_153202.4:c.1905+107G>C	NP_694882.1:n.1905+107G>C