Canonical Allele Identifier: CA1573505293

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112827162T= , CM000667.2:g.112827162T=	GRCh38
NC_000005.9:g.112162859T= , CM000667.1:g.112162859T=	GRCh37
NC_000005.8:g.112190758T=	NCBI36
NG_008481.4:g.139642T= , LRG_130:g.139642T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1408+5171T=	ENSP00000484935.2:n.1408+5171T=
ENST00000504915.3:c.1517T=	ENSP00000473355.2:p.Leu506=
ENST00000505084.2:n.1519T=
ENST00000505350.2:c.*1469T=	ENSP00000481752.1:n.*1469T=
ENST00000507379.6:c.1409T=	ENSP00000423224.2:p.Leu470=
ENST00000509732.6:c.1463T=	ENSP00000426541.2:p.Leu488=
ENST00000512211.7:c.1463T=	ENSP00000423828.3:p.Leu488=
ENST00000257430.9:c.1463T= MANE Select	ENSP00000257430.4:p.Leu488=
ENST00000257430.8:c.1463T=	ENSP00000257430.4:p.Leu488=
ENST00000502371.2:c.96+5171T=
ENST00000504915.2:c.152T=	ENSP00000473355.1:p.Leu51=
ENST00000507379.5:c.1409T=	ENSP00000423224.1:p.Leu470=
ENST00000508376.6:c.1463T=	ENSP00000427089.2:p.Leu488=
ENST00000508624.5:c.*785T=	ENSP00000424265.1:n.*785T=
ENST00000512211.6:c.1463T=	ENSP00000423828.2:p.Leu488=
NM_000038.5:c.1463T=	NP_000029.2:p.Leu488=
NM_001127510.2:c.1463T=	NP_001120982.1:p.Leu488=
NM_001127511.2:c.1409T=	NP_001120983.2:p.Leu470=
NM_001354895.1:c.1463T=	NP_001341824.1:p.Leu488=
NM_001354896.1:c.1517T=	NP_001341825.1:p.Leu506=
NM_001354897.1:c.1493T=	NP_001341826.1:p.Leu498=
NM_001354898.1:c.1388T=	NP_001341827.1:p.Leu463=
NM_001354899.1:c.1379T=	NP_001341828.1:p.Leu460=
NM_001354900.1:c.1340T=	NP_001341829.1:p.Leu447=
NM_001354901.1:c.1286T=	NP_001341830.1:p.Leu429=
NM_001354902.1:c.1190T=	NP_001341831.1:p.Leu397=
NM_001354903.1:c.1160T=	NP_001341832.1:p.Leu387=
NM_001354904.1:c.1085T=	NP_001341833.1:p.Leu362=
NM_001354905.1:c.983T=	NP_001341834.1:p.Leu328=
NM_001354906.1:c.614T=	NP_001341835.1:p.Leu205=
NM_000038.6:c.1463T= MANE Select	NP_000029.2:p.Leu488=
NM_001127510.3:c.1463T=	NP_001120982.1:p.Leu488=
NM_001127511.3:c.1409T=	NP_001120983.2:p.Leu470=
NM_001354895.2:c.1463T=	NP_001341824.1:p.Leu488=
NM_001354896.2:c.1517T=	NP_001341825.1:p.Leu506=
NM_001354897.2:c.1493T=	NP_001341826.1:p.Leu498=
NM_001354898.2:c.1388T=	NP_001341827.1:p.Leu463=
NM_001354899.2:c.1379T=	NP_001341828.1:p.Leu460=
NM_001354900.2:c.1340T=	NP_001341829.1:p.Leu447=
NM_001354901.2:c.1286T=	NP_001341830.1:p.Leu429=
NM_001354902.2:c.1190T=	NP_001341831.1:p.Leu397=
NM_001354903.2:c.1160T=	NP_001341832.1:p.Leu387=
NM_001354904.2:c.1085T=	NP_001341833.1:p.Leu362=
NM_001354905.2:c.983T=	NP_001341834.1:p.Leu328=
NM_001354906.2:c.614T=	NP_001341835.1:p.Leu205=