Canonical Allele Identifier: CA1573497127

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112821926C= , CM000667.2:g.112821926C=	GRCh38
NC_000005.9:g.112157623C= , CM000667.1:g.112157623C=	GRCh37
NC_000005.8:g.112185522C=	NCBI36
NG_008481.4:g.134406C= , LRG_130:g.134406C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1343C=	ENSP00000484935.2:p.Pro448=
ENST00000504915.3:c.1343C=	ENSP00000473355.2:p.Pro448=
ENST00000505084.2:n.1399C=
ENST00000505350.2:c.*1349C=	ENSP00000481752.1:n.*1349C=
ENST00000507379.6:c.1289C=	ENSP00000423224.2:p.Pro430=
ENST00000509732.6:c.1343C=	ENSP00000426541.2:p.Pro448=
ENST00000512211.7:c.1343C=	ENSP00000423828.3:p.Pro448=
ENST00000257430.9:c.1343C= MANE Select	ENSP00000257430.4:p.Pro448=
ENST00000257430.8:c.1343C=	ENSP00000257430.4:p.Pro448=
ENST00000502371.2:c.31C=
ENST00000507379.5:c.1289C=	ENSP00000423224.1:p.Pro430=
ENST00000508376.6:c.1343C=	ENSP00000427089.2:p.Pro448=
ENST00000508624.5:c.*665C=	ENSP00000424265.1:n.*665C=
ENST00000512211.6:c.1343C=	ENSP00000423828.2:p.Pro448=
NM_000038.5:c.1343C=	NP_000029.2:p.Pro448=
NM_001127510.2:c.1343C=	NP_001120982.1:p.Pro448=
NM_001127511.2:c.1289C=	NP_001120983.2:p.Pro430=
NM_001354895.1:c.1343C=	NP_001341824.1:p.Pro448=
NM_001354896.1:c.1343C=	NP_001341825.1:p.Pro448=
NM_001354897.1:c.1373C=	NP_001341826.1:p.Pro458=
NM_001354898.1:c.1268C=	NP_001341827.1:p.Pro423=
NM_001354899.1:c.1259C=	NP_001341828.1:p.Pro420=
NM_001354900.1:c.1166C=	NP_001341829.1:p.Pro389=
NM_001354901.1:c.1166C=	NP_001341830.1:p.Pro389=
NM_001354902.1:c.1070C=	NP_001341831.1:p.Pro357=
NM_001354903.1:c.1040C=	NP_001341832.1:p.Pro347=
NM_001354904.1:c.965C=	NP_001341833.1:p.Pro322=
NM_001354905.1:c.863C=	NP_001341834.1:p.Pro288=
NM_001354906.1:c.494C=	NP_001341835.1:p.Pro165=
NM_000038.6:c.1343C= MANE Select	NP_000029.2:p.Pro448=
NM_001127510.3:c.1343C=	NP_001120982.1:p.Pro448=
NM_001127511.3:c.1289C=	NP_001120983.2:p.Pro430=
NM_001354895.2:c.1343C=	NP_001341824.1:p.Pro448=
NM_001354896.2:c.1343C=	NP_001341825.1:p.Pro448=
NM_001354897.2:c.1373C=	NP_001341826.1:p.Pro458=
NM_001354898.2:c.1268C=	NP_001341827.1:p.Pro423=
NM_001354899.2:c.1259C=	NP_001341828.1:p.Pro420=
NM_001354900.2:c.1166C=	NP_001341829.1:p.Pro389=
NM_001354901.2:c.1166C=	NP_001341830.1:p.Pro389=
NM_001354902.2:c.1070C=	NP_001341831.1:p.Pro357=
NM_001354903.2:c.1040C=	NP_001341832.1:p.Pro347=
NM_001354904.2:c.965C=	NP_001341833.1:p.Pro322=
NM_001354905.2:c.863C=	NP_001341834.1:p.Pro288=
NM_001354906.2:c.494C=	NP_001341835.1:p.Pro165=