Canonical Allele Identifier: CA1573487964

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838968T= , CM000667.2:g.112838968T=	GRCh38
NC_000005.9:g.112174665T= , CM000667.1:g.112174665T=	GRCh37
NC_000005.8:g.112202564T=	NCBI36
NG_008481.4:g.151448T= , LRG_130:g.151448T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.3039T=	ENSP00000484935.2:n.3039T=
ENST00000504915.3:c.3428T=	ENSP00000473355.2:p.Val1143=
ENST00000505350.2:c.*3380T=	ENSP00000481752.1:n.*3380T=
ENST00000507379.6:c.3320T=	ENSP00000423224.2:p.Val1107=
ENST00000509732.6:c.3374T=	ENSP00000426541.2:p.Val1125=
ENST00000512211.7:c.3374T=	ENSP00000423828.3:p.Val1125=
ENST00000257430.9:c.3374T= MANE Select	ENSP00000257430.4:p.Val1125=
ENST00000257430.8:c.3374T=	ENSP00000257430.4:p.Val1125=
ENST00000502371.2:c.1727T=
ENST00000507379.5:c.3320T=	ENSP00000423224.1:p.Val1107=
ENST00000508376.6:c.3374T=	ENSP00000427089.2:p.Val1125=
ENST00000508624.5:c.*2696T=	ENSP00000424265.1:n.*2696T=
ENST00000512211.6:c.3374T=	ENSP00000423828.2:p.Val1125=
ENST00000520401.1:c.230+9996T=
NM_000038.5:c.3374T=	NP_000029.2:p.Val1125=
NM_001127510.2:c.3374T=	NP_001120982.1:p.Val1125=
NM_001127511.2:c.3320T=	NP_001120983.2:p.Val1107=
NM_001354895.1:c.3374T=	NP_001341824.1:p.Val1125=
NM_001354896.1:c.3428T=	NP_001341825.1:p.Val1143=
NM_001354897.1:c.3404T=	NP_001341826.1:p.Val1135=
NM_001354898.1:c.3299T=	NP_001341827.1:p.Val1100=
NM_001354899.1:c.3290T=	NP_001341828.1:p.Val1097=
NM_001354900.1:c.3251T=	NP_001341829.1:p.Val1084=
NM_001354901.1:c.3197T=	NP_001341830.1:p.Val1066=
NM_001354902.1:c.3101T=	NP_001341831.1:p.Val1034=
NM_001354903.1:c.3071T=	NP_001341832.1:p.Val1024=
NM_001354904.1:c.2996T=	NP_001341833.1:p.Val999=
NM_001354905.1:c.2894T=	NP_001341834.1:p.Val965=
NM_001354906.1:c.2525T=	NP_001341835.1:p.Val842=
NM_000038.6:c.3374T= MANE Select	NP_000029.2:p.Val1125=
NM_001127510.3:c.3374T=	NP_001120982.1:p.Val1125=
NM_001127511.3:c.3320T=	NP_001120983.2:p.Val1107=
NM_001354895.2:c.3374T=	NP_001341824.1:p.Val1125=
NM_001354896.2:c.3428T=	NP_001341825.1:p.Val1143=
NM_001354897.2:c.3404T=	NP_001341826.1:p.Val1135=
NM_001354898.2:c.3299T=	NP_001341827.1:p.Val1100=
NM_001354899.2:c.3290T=	NP_001341828.1:p.Val1097=
NM_001354900.2:c.3251T=	NP_001341829.1:p.Val1084=
NM_001354901.2:c.3197T=	NP_001341830.1:p.Val1066=
NM_001354902.2:c.3101T=	NP_001341831.1:p.Val1034=
NM_001354903.2:c.3071T=	NP_001341832.1:p.Val1024=
NM_001354904.2:c.2996T=	NP_001341833.1:p.Val999=
NM_001354905.2:c.2894T=	NP_001341834.1:p.Val965=
NM_001354906.2:c.2525T=	NP_001341835.1:p.Val842=