Canonical Allele Identifier: CA1573484584

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112815516C= , CM000667.2:g.112815516C=	GRCh38
NC_000005.9:g.112151213C= , CM000667.1:g.112151213C=	GRCh37
NC_000005.8:g.112179112C=	NCBI36
NG_008481.4:g.127996C= , LRG_130:g.127996C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000038.6:c.856C= MANE Select	NP_000029.2:p.His286=
ENST00000257430.9:c.856C= MANE Select	ENSP00000257430.4:p.His286=
NM_000038.5:c.856C=	NP_000029.2:p.His286=
NM_001127510.2:c.856C=	NP_001120982.1:p.His286=
NM_001127510.3:c.856C=	NP_001120982.1:p.His286=
NM_001127511.2:c.802C=	NP_001120983.2:p.His268=
NM_001127511.3:c.802C=	NP_001120983.2:p.His268=
NM_001354895.1:c.856C=	NP_001341824.1:p.His286=
NM_001354895.2:c.856C=	NP_001341824.1:p.His286=
NM_001354896.1:c.856C=	NP_001341825.1:p.His286=
NM_001354896.2:c.856C=	NP_001341825.1:p.His286=
NM_001354897.1:c.886C=	NP_001341826.1:p.His296=
NM_001354897.2:c.886C=	NP_001341826.1:p.His296=
NM_001354898.1:c.781C=	NP_001341827.1:p.His261=
NM_001354898.2:c.781C=	NP_001341827.1:p.His261=
NM_001354899.1:c.772C=	NP_001341828.1:p.His258=
NM_001354899.2:c.772C=	NP_001341828.1:p.His258=
NM_001354900.1:c.679C=	NP_001341829.1:p.His227=
NM_001354900.2:c.679C=	NP_001341829.1:p.His227=
NM_001354901.1:c.679C=	NP_001341830.1:p.His227=
NM_001354901.2:c.679C=	NP_001341830.1:p.His227=
NM_001354902.1:c.886C=	NP_001341831.1:p.His296=
NM_001354902.2:c.886C=	NP_001341831.1:p.His296=
NM_001354903.1:c.856C=	NP_001341832.1:p.His286=
NM_001354903.2:c.856C=	NP_001341832.1:p.His286=
NM_001354904.1:c.781C=	NP_001341833.1:p.His261=
NM_001354904.2:c.781C=	NP_001341833.1:p.His261=
NM_001354905.1:c.679C=	NP_001341834.1:p.His227=
NM_001354905.2:c.679C=	NP_001341834.1:p.His227=
NM_001354906.1:c.7C=	NP_001341835.1:p.His3=
NM_001354906.2:c.7C=	NP_001341835.1:p.His3=
ENST00000257430.8:c.856C=	ENSP00000257430.4:p.His286=
ENST00000502371.3:c.856C=	ENSP00000484935.2:p.His286=
ENST00000504915.3:c.856C=	ENSP00000473355.2:p.His286=
ENST00000505084.2:n.912C=
ENST00000505350.2:c.*862C=	ENSP00000481752.1:n.*862C=
ENST00000507379.5:c.802C=	ENSP00000423224.1:p.His268=
ENST00000507379.6:c.802C=	ENSP00000423224.2:p.His268=
ENST00000508376.6:c.856C=	ENSP00000427089.2:p.His286=
ENST00000508624.5:c.*178C=	ENSP00000424265.1:n.*178C=
ENST00000509732.6:c.856C=	ENSP00000426541.2:p.His286=
ENST00000512211.6:c.856C=	ENSP00000423828.2:p.His286=
ENST00000512211.7:c.856C=	ENSP00000423828.3:p.His286=