Canonical Allele Identifier: CA408104686

Gene: ADAM33

Linked Data

• COSMIC: COSM3748148
• MyVariant Identifiers: chr20:g.3652076T>C (hg19) ; chr20:g.3671429T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671429T>C , CM000682.2:g.3671429T>C	GRCh38
NC_000020.10:g.3652076T>C , CM000682.1:g.3652076T>C	GRCh37
NC_000020.9:g.3600076T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1973A>G MANE Select	ENSP00000348912.3:p.His658Arg
ENST00000350009.6:c.1906-84A>G	ENSP00000322550.5:n.1906-84A>G
ENST00000356518.6:c.1973A>G	ENSP00000348912.2:p.His658Arg
ENST00000379861.8:c.1973A>G	ENSP00000369190.4:p.His658Arg
ENST00000466620.5:n.1545-84A>G
ENST00000617732.1:c.*660A>G	ENSP00000483343.1:n.*660A>G
ENST00000619289.4:c.1613A>G	ENSP00000484600.1:p.His538Arg
NM_001282447.1:c.1973A>G	NP_001269376.1:p.His658Arg
NM_025220.3:c.1973A>G	NP_079496.1:p.His658Arg
NM_153202.2:c.1906-84A>G	NP_694882.1:n.1906-84A>G
XM_005260843.1:c.2012A>G	XP_005260900.1:p.His671Arg
XM_006723639.1:c.2012A>G	XP_006723702.1:p.His671Arg
XM_006723640.1:c.2003A>G	XP_006723703.1:p.His668Arg
XM_011529366.1:c.2009A>G	XP_011527668.1:p.His670Arg
XM_011529367.1:c.1970A>G	XP_011527669.1:p.His657Arg
XM_011529368.1:c.1945-84A>G	XP_011527670.1:n.1945-84A>G
XM_011529369.1:c.*72A>G	XP_011527671.1:n.*72A>G
XM_011529370.1:c.*5-84A>G	XP_011527672.1:n.*5-84A>G
XM_011529373.1:c.1010A>G	XP_011527675.1:p.His337Arg
XR_937151.1:n.2116A>G
XR_937152.1:n.2116A>G
XR_937153.1:n.1997A>G
XR_937154.1:n.1997A>G
XR_937155.1:n.1918A>G
XR_937157.1:n.1920A>G
NM_001282447.2:c.1973A>G	NP_001269376.1:p.His658Arg
NM_025220.4:c.1973A>G	NP_079496.1:p.His658Arg
NM_153202.3:c.1906-84A>G	NP_694882.1:n.1906-84A>G
XM_011529373.2:c.1010A>G	XP_011527675.1:p.His337Arg
XR_001754405.1:n.2084A>G
XR_002958534.1:n.2193A>G
NM_001282447.3:c.1973A>G	NP_001269376.1:p.His658Arg
NM_025220.5:c.1973A>G MANE Select	NP_079496.1:p.His658Arg
NM_153202.4:c.1906-84A>G	NP_694882.1:n.1906-84A>G