Canonical Allele Identifier: CA408104794

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652124C>G (hg19) ; chr20:g.3671477C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671477C>G , CM000682.2:g.3671477C>G	GRCh38
NC_000020.10:g.3652124C>G , CM000682.1:g.3652124C>G	GRCh37
NC_000020.9:g.3600124C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1925G>C MANE Select	ENSP00000348912.3:p.Cys642Ser
ENST00000350009.6:c.1905+104G>C	ENSP00000322550.5:n.1905+104G>C
ENST00000356518.6:c.1925G>C	ENSP00000348912.2:p.Cys642Ser
ENST00000379861.8:c.1925G>C	ENSP00000369190.4:p.Cys642Ser
ENST00000466620.5:n.1544+104G>C
ENST00000617732.1:c.*632-20G>C	ENSP00000483343.1:n.*632-20G>C
ENST00000619289.4:c.1565G>C	ENSP00000484600.1:p.Cys522Ser
NM_001282447.1:c.1925G>C	NP_001269376.1:p.Cys642Ser
NM_025220.3:c.1925G>C	NP_079496.1:p.Cys642Ser
NM_153202.2:c.1905+104G>C	NP_694882.1:n.1905+104G>C
XM_005260843.1:c.1964G>C	XP_005260900.1:p.Cys655Ser
XM_006723639.1:c.1964G>C	XP_006723702.1:p.Cys655Ser
XM_006723640.1:c.1955G>C	XP_006723703.1:p.Cys652Ser
XM_011529366.1:c.1961G>C	XP_011527668.1:p.Cys654Ser
XM_011529367.1:c.1922G>C	XP_011527669.1:p.Cys641Ser
XM_011529368.1:c.1944+104G>C	XP_011527670.1:n.1944+104G>C
XM_011529369.1:c.*24G>C	XP_011527671.1:n.*24G>C
XM_011529370.1:c.*4+104G>C	XP_011527672.1:n.*4+104G>C
XM_011529373.1:c.962G>C	XP_011527675.1:p.Cys321Ser
XR_937151.1:n.2068G>C
XR_937152.1:n.2068G>C
XR_937153.1:n.1949G>C
XR_937154.1:n.1949G>C
XR_937155.1:n.1870G>C
XR_937157.1:n.1872G>C
NM_001282447.2:c.1925G>C	NP_001269376.1:p.Cys642Ser
NM_025220.4:c.1925G>C	NP_079496.1:p.Cys642Ser
NM_153202.3:c.1905+104G>C	NP_694882.1:n.1905+104G>C
XM_011529373.2:c.962G>C	XP_011527675.1:p.Cys321Ser
XR_001754405.1:n.2036G>C
XR_002958534.1:n.2145G>C
NM_001282447.3:c.1925G>C	NP_001269376.1:p.Cys642Ser
NM_025220.5:c.1925G>C MANE Select	NP_079496.1:p.Cys642Ser
NM_153202.4:c.1905+104G>C	NP_694882.1:n.1905+104G>C