Canonical Allele Identifier: CA1573471014

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840299G= , CM000667.2:g.112840299G=	GRCh38
NC_000005.9:g.112175996G= , CM000667.1:g.112175996G=	GRCh37
NC_000005.8:g.112203895G=	NCBI36
NG_008481.4:g.152779G= , LRG_130:g.152779G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4759G=	ENSP00000473355.2:p.Asp1587=
ENST00000505350.2:c.*4711G=	ENSP00000481752.1:n.*4711G=
ENST00000507379.6:c.4651G=	ENSP00000423224.2:p.Asp1551=
ENST00000509732.6:c.4705G=	ENSP00000426541.2:p.Asp1569=
ENST00000512211.7:c.4705G=	ENSP00000423828.3:p.Asp1569=
ENST00000257430.9:c.4705G= MANE Select	ENSP00000257430.4:p.Asp1569=
ENST00000257430.8:c.4705G=	ENSP00000257430.4:p.Asp1569=
ENST00000508376.6:c.4705G=	ENSP00000427089.2:p.Asp1569=
ENST00000508624.5:c.*4027G=	ENSP00000424265.1:n.*4027G=
ENST00000520401.1:c.230+11327G=
NM_000038.5:c.4705G=	NP_000029.2:p.Asp1569=
NM_001127510.2:c.4705G=	NP_001120982.1:p.Asp1569=
NM_001127511.2:c.4651G=	NP_001120983.2:p.Asp1551=
NM_001354895.1:c.4705G=	NP_001341824.1:p.Asp1569=
NM_001354896.1:c.4759G=	NP_001341825.1:p.Asp1587=
NM_001354897.1:c.4735G=	NP_001341826.1:p.Asp1579=
NM_001354898.1:c.4630G=	NP_001341827.1:p.Asp1544=
NM_001354899.1:c.4621G=	NP_001341828.1:p.Asp1541=
NM_001354900.1:c.4582G=	NP_001341829.1:p.Asp1528=
NM_001354901.1:c.4528G=	NP_001341830.1:p.Asp1510=
NM_001354902.1:c.4432G=	NP_001341831.1:p.Asp1478=
NM_001354903.1:c.4402G=	NP_001341832.1:p.Asp1468=
NM_001354904.1:c.4327G=	NP_001341833.1:p.Asp1443=
NM_001354905.1:c.4225G=	NP_001341834.1:p.Asp1409=
NM_001354906.1:c.3856G=	NP_001341835.1:p.Asp1286=
NM_000038.6:c.4705G= MANE Select	NP_000029.2:p.Asp1569=
NM_001127510.3:c.4705G=	NP_001120982.1:p.Asp1569=
NM_001127511.3:c.4651G=	NP_001120983.2:p.Asp1551=
NM_001354895.2:c.4705G=	NP_001341824.1:p.Asp1569=
NM_001354896.2:c.4759G=	NP_001341825.1:p.Asp1587=
NM_001354897.2:c.4735G=	NP_001341826.1:p.Asp1579=
NM_001354898.2:c.4630G=	NP_001341827.1:p.Asp1544=
NM_001354899.2:c.4621G=	NP_001341828.1:p.Asp1541=
NM_001354900.2:c.4582G=	NP_001341829.1:p.Asp1528=
NM_001354901.2:c.4528G=	NP_001341830.1:p.Asp1510=
NM_001354902.2:c.4432G=	NP_001341831.1:p.Asp1478=
NM_001354903.2:c.4402G=	NP_001341832.1:p.Asp1468=
NM_001354904.2:c.4327G=	NP_001341833.1:p.Asp1443=
NM_001354905.2:c.4225G=	NP_001341834.1:p.Asp1409=
NM_001354906.2:c.3856G=	NP_001341835.1:p.Asp1286=