Canonical Allele Identifier: CA1573472646

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840547T= , CM000667.2:g.112840547T=	GRCh38
NC_000005.9:g.112176244T= , CM000667.1:g.112176244T=	GRCh37
NC_000005.8:g.112204143T=	NCBI36
NG_008481.4:g.153027T= , LRG_130:g.153027T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5007T=	ENSP00000473355.2:p.Phe1669=
ENST00000505350.2:c.*4959T=	ENSP00000481752.1:n.*4959T=
ENST00000507379.6:c.4899T=	ENSP00000423224.2:p.Phe1633=
ENST00000509732.6:c.4953T=	ENSP00000426541.2:p.Phe1651=
ENST00000512211.7:c.4953T=	ENSP00000423828.3:p.Phe1651=
ENST00000257430.9:c.4953T= MANE Select	ENSP00000257430.4:p.Phe1651=
ENST00000257430.8:c.4953T=	ENSP00000257430.4:p.Phe1651=
ENST00000508376.6:c.4953T=	ENSP00000427089.2:p.Phe1651=
ENST00000508624.5:c.*4275T=	ENSP00000424265.1:n.*4275T=
ENST00000520401.1:c.230+11575T=
NM_000038.5:c.4953T=	NP_000029.2:p.Phe1651=
NM_001127510.2:c.4953T=	NP_001120982.1:p.Phe1651=
NM_001127511.2:c.4899T=	NP_001120983.2:p.Phe1633=
NM_001354895.1:c.4953T=	NP_001341824.1:p.Phe1651=
NM_001354896.1:c.5007T=	NP_001341825.1:p.Phe1669=
NM_001354897.1:c.4983T=	NP_001341826.1:p.Phe1661=
NM_001354898.1:c.4878T=	NP_001341827.1:p.Phe1626=
NM_001354899.1:c.4869T=	NP_001341828.1:p.Phe1623=
NM_001354900.1:c.4830T=	NP_001341829.1:p.Phe1610=
NM_001354901.1:c.4776T=	NP_001341830.1:p.Phe1592=
NM_001354902.1:c.4680T=	NP_001341831.1:p.Phe1560=
NM_001354903.1:c.4650T=	NP_001341832.1:p.Phe1550=
NM_001354904.1:c.4575T=	NP_001341833.1:p.Phe1525=
NM_001354905.1:c.4473T=	NP_001341834.1:p.Phe1491=
NM_001354906.1:c.4104T=	NP_001341835.1:p.Phe1368=
NM_000038.6:c.4953T= MANE Select	NP_000029.2:p.Phe1651=
NM_001127510.3:c.4953T=	NP_001120982.1:p.Phe1651=
NM_001127511.3:c.4899T=	NP_001120983.2:p.Phe1633=
NM_001354895.2:c.4953T=	NP_001341824.1:p.Phe1651=
NM_001354896.2:c.5007T=	NP_001341825.1:p.Phe1669=
NM_001354897.2:c.4983T=	NP_001341826.1:p.Phe1661=
NM_001354898.2:c.4878T=	NP_001341827.1:p.Phe1626=
NM_001354899.2:c.4869T=	NP_001341828.1:p.Phe1623=
NM_001354900.2:c.4830T=	NP_001341829.1:p.Phe1610=
NM_001354901.2:c.4776T=	NP_001341830.1:p.Phe1592=
NM_001354902.2:c.4680T=	NP_001341831.1:p.Phe1560=
NM_001354903.2:c.4650T=	NP_001341832.1:p.Phe1550=
NM_001354904.2:c.4575T=	NP_001341833.1:p.Phe1525=
NM_001354905.2:c.4473T=	NP_001341834.1:p.Phe1491=
NM_001354906.2:c.4104T=	NP_001341835.1:p.Phe1368=