Canonical Allele Identifier: CA2537725554

Gene: CD46 MIR29B2CHG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207785152_207785153del , CM000663.2:g.207785152_207785153del	GRCh38
NC_000001.10:g.207958497_207958498del , CM000663.1:g.207958497_207958498del	GRCh37
NC_000001.9:g.206025120_206025121del	NCBI36
NG_009296.1:g.38096_38097del , LRG_155:g.38096_38097del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490278.2:n.2192+46_2192+47del (CD46)
ENST00000496723.2:n.1769+46_1769+47del (CD46)
ENST00000636114.2:n.2711+46_2711+47del (CD46)
ENST00000695777.1:c.1018+46_1018+47del (CD46)	ENSP00000512167.1:n.1018+46_1018+47del
ENST00000695778.1:c.973+46_973+47del (CD46)	ENSP00000512168.1:n.973+46_973+47del
ENST00000695779.1:n.1735+46_1735+47del (CD46)
ENST00000695780.1:c.938-504_938-503del (CD46)	ENSP00000512169.1:n.938-504_938-503del
ENST00000695781.1:c.*101+46_*101+47del (CD46)	ENSP00000512170.1:n.*101+46_*101+47del
ENST00000695782.1:c.973+46_973+47del (CD46)	ENSP00000512171.1:n.973+46_973+47del
ENST00000695783.1:n.4386+46_4386+47del (CD46)
ENST00000695784.1:c.*144+46_*144+47del (CD46)	ENSP00000512172.1:n.*144+46_*144+47del
ENST00000695786.1:n.940+46_940+47del (CD46)
ENST00000695787.1:n.2376+46_2376+47del (CD46)
ENST00000695788.1:n.597+46_597+47del (CD46)
ENST00000695789.1:n.2315_2316del (CD46)
ENST00000695790.1:n.2304_2305del (CD46)
ENST00000367042.6:c.1018+46_1018+47del (CD46) MANE Select	ENSP00000356009.1:n.1018+46_1018+47del
ENST00000636114.1:n.772+46_772+47del (CD46)
ENST00000322875.8:c.1063+46_1063+47del (CD46)	ENSP00000313875.4:n.1063+46_1063+47del
ENST00000322918.9:c.973+46_973+47del (CD46)	ENSP00000314664.5:n.973+46_973+47del
ENST00000354848.5:c.1018+46_1018+47del (CD46)	ENSP00000346912.1:n.1018+46_1018+47del
ENST00000357714.5:c.973+46_973+47del (CD46)	ENSP00000350346.1:n.973+46_973+47del
ENST00000358170.6:c.1063+46_1063+47del (CD46)	ENSP00000350893.2:n.1063+46_1063+47del
ENST00000360212.6:c.931+46_931+47del (CD46)	ENSP00000353342.2:n.931+46_931+47del
ENST00000367041.5:c.973+46_973+47del (CD46)	ENSP00000356008.1:n.973+46_973+47del
ENST00000367042.5:c.1018+46_1018+47del (CD46)	ENSP00000356009.1:n.1018+46_1018+47del
ENST00000367047.5:c.874+46_874+47del (CD46)	ENSP00000356014.1:n.874+46_874+47del
ENST00000462968.2:c.99+46_99+47del (CD46)
ENST00000469535.5:n.5767+46_5767+47del (CD46)
ENST00000471987.1:n.128+46_128+47del (CD46)
ENST00000480003.5:c.976+46_976+47del (CD46)	ENSP00000418471.1:n.976+46_976+47del
ENST00000488596.5:n.397+46_397+47del (CD46)
NM_002389.4:c.1063+46_1063+47del , LRG_155t1:c.1063+46_1063+47del (CD46)	NP_002380.3:n.1063+46_1063+47del
NM_153826.3:c.1018+46_1018+47del (CD46)	NP_722548.1:n.1018+46_1018+47del
NM_172350.2:c.973+46_973+47del (CD46)	NP_758860.1:n.973+46_973+47del
NM_172351.2:c.1018+46_1018+47del (CD46)	NP_758861.1:n.1018+46_1018+47del
NM_172352.2:c.973+46_973+47del (CD46)	NP_758862.1:n.973+46_973+47del
NM_172353.2:c.973+46_973+47del (CD46)	NP_758863.1:n.973+46_973+47del
NM_172359.2:c.1063+46_1063+47del (CD46)	NP_758869.1:n.1063+46_1063+47del
NM_172361.2:c.931+46_931+47del (CD46)	NP_758871.1:n.931+46_931+47del
XM_011509563.1:c.1021+46_1021+47del (CD46)	XP_011507865.1:n.1021+46_1021+47del
XM_011509564.1:c.976+46_976+47del (CD46)	XP_011507866.1:n.976+46_976+47del
XR_922496.1:n.7666+20854_7666+20855del (MIR29B2CHG)
XR_922497.1:n.6306-22163_6306-22162del (MIR29B2CHG)
NM_172355.2:c.976+46_976+47del (CD46)	NP_758865.1:n.976+46_976+47del
NM_172356.2:c.976+46_976+47del (CD46)	NP_758866.1:n.976+46_976+47del
NM_172357.2:c.931+46_931+47del (CD46)	NP_758867.1:n.931+46_931+47del
NM_172358.2:c.1018+46_1018+47del (CD46)	NP_758868.1:n.1018+46_1018+47del
XM_011509563.2:c.1021+46_1021+47del (CD46)	XP_011507865.1:n.1021+46_1021+47del
XM_017001308.2:c.1021+46_1021+47del (CD46)	XP_016856797.1:n.1021+46_1021+47del
XR_001737177.2:n.2169+46_2169+47del (CD46)
XR_002956621.1:n.2707+46_2707+47del (CD46)
XR_002956622.1:n.2707+46_2707+47del (CD46)
NM_153826.4:c.1018+46_1018+47del (CD46)	NP_722548.1:n.1018+46_1018+47del
NM_172350.3:c.973+46_973+47del (CD46)	NP_758860.1:n.973+46_973+47del
NM_172351.3:c.1018+46_1018+47del (CD46) MANE Select	NP_758861.1:n.1018+46_1018+47del
NM_172352.3:c.973+46_973+47del (CD46)	NP_758862.1:n.973+46_973+47del
NM_172353.3:c.973+46_973+47del (CD46)	NP_758863.1:n.973+46_973+47del
NM_172355.3:c.976+46_976+47del (CD46)	NP_758865.1:n.976+46_976+47del
NM_172356.3:c.976+46_976+47del (CD46)	NP_758866.1:n.976+46_976+47del
NM_172357.3:c.931+46_931+47del (CD46)	NP_758867.1:n.931+46_931+47del
NM_172358.3:c.1018+46_1018+47del (CD46)	NP_758868.1:n.1018+46_1018+47del
NM_172359.3:c.1063+46_1063+47del (CD46)	NP_758869.1:n.1063+46_1063+47del
NM_172361.3:c.931+46_931+47del (CD46)	NP_758871.1:n.931+46_931+47del