Canonical Allele Identifier: CA1573475226

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840868T= , CM000667.2:g.112840868T=	GRCh38
NC_000005.9:g.112176565T= , CM000667.1:g.112176565T=	GRCh37
NC_000005.8:g.112204464T=	NCBI36
NG_008481.4:g.153348T= , LRG_130:g.153348T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5328T=	ENSP00000473355.2:p.Ser1776=
ENST00000505350.2:c.*5280T=	ENSP00000481752.1:n.*5280T=
ENST00000507379.6:c.5220T=	ENSP00000423224.2:p.Ser1740=
ENST00000509732.6:c.5274T=	ENSP00000426541.2:p.Ser1758=
ENST00000512211.7:c.5274T=	ENSP00000423828.3:p.Ser1758=
ENST00000257430.9:c.5274T= MANE Select	ENSP00000257430.4:p.Ser1758=
ENST00000257430.8:c.5274T=	ENSP00000257430.4:p.Ser1758=
ENST00000508376.6:c.5274T=	ENSP00000427089.2:p.Ser1758=
ENST00000508624.5:c.*4596T=	ENSP00000424265.1:n.*4596T=
ENST00000520401.1:c.230+11896T=
NM_000038.5:c.5274T=	NP_000029.2:p.Ser1758=
NM_001127510.2:c.5274T=	NP_001120982.1:p.Ser1758=
NM_001127511.2:c.5220T=	NP_001120983.2:p.Ser1740=
NM_001354895.1:c.5274T=	NP_001341824.1:p.Ser1758=
NM_001354896.1:c.5328T=	NP_001341825.1:p.Ser1776=
NM_001354897.1:c.5304T=	NP_001341826.1:p.Ser1768=
NM_001354898.1:c.5199T=	NP_001341827.1:p.Ser1733=
NM_001354899.1:c.5190T=	NP_001341828.1:p.Ser1730=
NM_001354900.1:c.5151T=	NP_001341829.1:p.Ser1717=
NM_001354901.1:c.5097T=	NP_001341830.1:p.Ser1699=
NM_001354902.1:c.5001T=	NP_001341831.1:p.Ser1667=
NM_001354903.1:c.4971T=	NP_001341832.1:p.Ser1657=
NM_001354904.1:c.4896T=	NP_001341833.1:p.Ser1632=
NM_001354905.1:c.4794T=	NP_001341834.1:p.Ser1598=
NM_001354906.1:c.4425T=	NP_001341835.1:p.Ser1475=
NM_000038.6:c.5274T= MANE Select	NP_000029.2:p.Ser1758=
NM_001127510.3:c.5274T=	NP_001120982.1:p.Ser1758=
NM_001127511.3:c.5220T=	NP_001120983.2:p.Ser1740=
NM_001354895.2:c.5274T=	NP_001341824.1:p.Ser1758=
NM_001354896.2:c.5328T=	NP_001341825.1:p.Ser1776=
NM_001354897.2:c.5304T=	NP_001341826.1:p.Ser1768=
NM_001354898.2:c.5199T=	NP_001341827.1:p.Ser1733=
NM_001354899.2:c.5190T=	NP_001341828.1:p.Ser1730=
NM_001354900.2:c.5151T=	NP_001341829.1:p.Ser1717=
NM_001354901.2:c.5097T=	NP_001341830.1:p.Ser1699=
NM_001354902.2:c.5001T=	NP_001341831.1:p.Ser1667=
NM_001354903.2:c.4971T=	NP_001341832.1:p.Ser1657=
NM_001354904.2:c.4896T=	NP_001341833.1:p.Ser1632=
NM_001354905.2:c.4794T=	NP_001341834.1:p.Ser1598=
NM_001354906.2:c.4425T=	NP_001341835.1:p.Ser1475=