Canonical Allele Identifier: CA1573474833

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840816T= , CM000667.2:g.112840816T=	GRCh38
NC_000005.9:g.112176513T= , CM000667.1:g.112176513T=	GRCh37
NC_000005.8:g.112204412T=	NCBI36
NG_008481.4:g.153296T= , LRG_130:g.153296T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5276T=	ENSP00000473355.2:p.Phe1759=
ENST00000505350.2:c.*5228T=	ENSP00000481752.1:n.*5228T=
ENST00000507379.6:c.5168T=	ENSP00000423224.2:p.Phe1723=
ENST00000509732.6:c.5222T=	ENSP00000426541.2:p.Phe1741=
ENST00000512211.7:c.5222T=	ENSP00000423828.3:p.Phe1741=
ENST00000257430.9:c.5222T= MANE Select	ENSP00000257430.4:p.Phe1741=
ENST00000257430.8:c.5222T=	ENSP00000257430.4:p.Phe1741=
ENST00000508376.6:c.5222T=	ENSP00000427089.2:p.Phe1741=
ENST00000508624.5:c.*4544T=	ENSP00000424265.1:n.*4544T=
ENST00000520401.1:c.230+11844T=
NM_000038.5:c.5222T=	NP_000029.2:p.Phe1741=
NM_001127510.2:c.5222T=	NP_001120982.1:p.Phe1741=
NM_001127511.2:c.5168T=	NP_001120983.2:p.Phe1723=
NM_001354895.1:c.5222T=	NP_001341824.1:p.Phe1741=
NM_001354896.1:c.5276T=	NP_001341825.1:p.Phe1759=
NM_001354897.1:c.5252T=	NP_001341826.1:p.Phe1751=
NM_001354898.1:c.5147T=	NP_001341827.1:p.Phe1716=
NM_001354899.1:c.5138T=	NP_001341828.1:p.Phe1713=
NM_001354900.1:c.5099T=	NP_001341829.1:p.Phe1700=
NM_001354901.1:c.5045T=	NP_001341830.1:p.Phe1682=
NM_001354902.1:c.4949T=	NP_001341831.1:p.Phe1650=
NM_001354903.1:c.4919T=	NP_001341832.1:p.Phe1640=
NM_001354904.1:c.4844T=	NP_001341833.1:p.Phe1615=
NM_001354905.1:c.4742T=	NP_001341834.1:p.Phe1581=
NM_001354906.1:c.4373T=	NP_001341835.1:p.Phe1458=
NM_000038.6:c.5222T= MANE Select	NP_000029.2:p.Phe1741=
NM_001127510.3:c.5222T=	NP_001120982.1:p.Phe1741=
NM_001127511.3:c.5168T=	NP_001120983.2:p.Phe1723=
NM_001354895.2:c.5222T=	NP_001341824.1:p.Phe1741=
NM_001354896.2:c.5276T=	NP_001341825.1:p.Phe1759=
NM_001354897.2:c.5252T=	NP_001341826.1:p.Phe1751=
NM_001354898.2:c.5147T=	NP_001341827.1:p.Phe1716=
NM_001354899.2:c.5138T=	NP_001341828.1:p.Phe1713=
NM_001354900.2:c.5099T=	NP_001341829.1:p.Phe1700=
NM_001354901.2:c.5045T=	NP_001341830.1:p.Phe1682=
NM_001354902.2:c.4949T=	NP_001341831.1:p.Phe1650=
NM_001354903.2:c.4919T=	NP_001341832.1:p.Phe1640=
NM_001354904.2:c.4844T=	NP_001341833.1:p.Phe1615=
NM_001354905.2:c.4742T=	NP_001341834.1:p.Phe1581=
NM_001354906.2:c.4373T=	NP_001341835.1:p.Phe1458=