Canonical Allele Identifier: CA1573497147

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112821931G= , CM000667.2:g.112821931G=	GRCh38
NC_000005.9:g.112157628G= , CM000667.1:g.112157628G=	GRCh37
NC_000005.8:g.112185527G=	NCBI36
NG_008481.4:g.134411G= , LRG_130:g.134411G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1348G=	ENSP00000484935.2:p.Val450=
ENST00000504915.3:c.1348G=	ENSP00000473355.2:p.Val450=
ENST00000505084.2:n.1404G=
ENST00000505350.2:c.*1354G=	ENSP00000481752.1:n.*1354G=
ENST00000507379.6:c.1294G=	ENSP00000423224.2:p.Val432=
ENST00000509732.6:c.1348G=	ENSP00000426541.2:p.Val450=
ENST00000512211.7:c.1348G=	ENSP00000423828.3:p.Val450=
ENST00000257430.9:c.1348G= MANE Select	ENSP00000257430.4:p.Val450=
ENST00000257430.8:c.1348G=	ENSP00000257430.4:p.Val450=
ENST00000502371.2:c.36G=
ENST00000507379.5:c.1294G=	ENSP00000423224.1:p.Val432=
ENST00000508376.6:c.1348G=	ENSP00000427089.2:p.Val450=
ENST00000508624.5:c.*670G=	ENSP00000424265.1:n.*670G=
ENST00000512211.6:c.1348G=	ENSP00000423828.2:p.Val450=
NM_000038.5:c.1348G=	NP_000029.2:p.Val450=
NM_001127510.2:c.1348G=	NP_001120982.1:p.Val450=
NM_001127511.2:c.1294G=	NP_001120983.2:p.Val432=
NM_001354895.1:c.1348G=	NP_001341824.1:p.Val450=
NM_001354896.1:c.1348G=	NP_001341825.1:p.Val450=
NM_001354897.1:c.1378G=	NP_001341826.1:p.Val460=
NM_001354898.1:c.1273G=	NP_001341827.1:p.Val425=
NM_001354899.1:c.1264G=	NP_001341828.1:p.Val422=
NM_001354900.1:c.1171G=	NP_001341829.1:p.Val391=
NM_001354901.1:c.1171G=	NP_001341830.1:p.Val391=
NM_001354902.1:c.1075G=	NP_001341831.1:p.Val359=
NM_001354903.1:c.1045G=	NP_001341832.1:p.Val349=
NM_001354904.1:c.970G=	NP_001341833.1:p.Val324=
NM_001354905.1:c.868G=	NP_001341834.1:p.Val290=
NM_001354906.1:c.499G=	NP_001341835.1:p.Val167=
NM_000038.6:c.1348G= MANE Select	NP_000029.2:p.Val450=
NM_001127510.3:c.1348G=	NP_001120982.1:p.Val450=
NM_001127511.3:c.1294G=	NP_001120983.2:p.Val432=
NM_001354895.2:c.1348G=	NP_001341824.1:p.Val450=
NM_001354896.2:c.1348G=	NP_001341825.1:p.Val450=
NM_001354897.2:c.1378G=	NP_001341826.1:p.Val460=
NM_001354898.2:c.1273G=	NP_001341827.1:p.Val425=
NM_001354899.2:c.1264G=	NP_001341828.1:p.Val422=
NM_001354900.2:c.1171G=	NP_001341829.1:p.Val391=
NM_001354901.2:c.1171G=	NP_001341830.1:p.Val391=
NM_001354902.2:c.1075G=	NP_001341831.1:p.Val359=
NM_001354903.2:c.1045G=	NP_001341832.1:p.Val349=
NM_001354904.2:c.970G=	NP_001341833.1:p.Val324=
NM_001354905.2:c.868G=	NP_001341834.1:p.Val290=
NM_001354906.2:c.499G=	NP_001341835.1:p.Val167=