Canonical Allele Identifier: CA1573473616

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840666C= , CM000667.2:g.112840666C=	GRCh38
NC_000005.9:g.112176363C= , CM000667.1:g.112176363C=	GRCh37
NC_000005.8:g.112204262C=	NCBI36
NG_008481.4:g.153146C= , LRG_130:g.153146C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5126C=	ENSP00000473355.2:p.Pro1709=
ENST00000505350.2:c.*5078C=	ENSP00000481752.1:n.*5078C=
ENST00000507379.6:c.5018C=	ENSP00000423224.2:p.Pro1673=
ENST00000509732.6:c.5072C=	ENSP00000426541.2:p.Pro1691=
ENST00000512211.7:c.5072C=	ENSP00000423828.3:p.Pro1691=
ENST00000257430.9:c.5072C= MANE Select	ENSP00000257430.4:p.Pro1691=
ENST00000257430.8:c.5072C=	ENSP00000257430.4:p.Pro1691=
ENST00000508376.6:c.5072C=	ENSP00000427089.2:p.Pro1691=
ENST00000508624.5:c.*4394C=	ENSP00000424265.1:n.*4394C=
ENST00000520401.1:c.230+11694C=
NM_000038.5:c.5072C=	NP_000029.2:p.Pro1691=
NM_001127510.2:c.5072C=	NP_001120982.1:p.Pro1691=
NM_001127511.2:c.5018C=	NP_001120983.2:p.Pro1673=
NM_001354895.1:c.5072C=	NP_001341824.1:p.Pro1691=
NM_001354896.1:c.5126C=	NP_001341825.1:p.Pro1709=
NM_001354897.1:c.5102C=	NP_001341826.1:p.Pro1701=
NM_001354898.1:c.4997C=	NP_001341827.1:p.Pro1666=
NM_001354899.1:c.4988C=	NP_001341828.1:p.Pro1663=
NM_001354900.1:c.4949C=	NP_001341829.1:p.Pro1650=
NM_001354901.1:c.4895C=	NP_001341830.1:p.Pro1632=
NM_001354902.1:c.4799C=	NP_001341831.1:p.Pro1600=
NM_001354903.1:c.4769C=	NP_001341832.1:p.Pro1590=
NM_001354904.1:c.4694C=	NP_001341833.1:p.Pro1565=
NM_001354905.1:c.4592C=	NP_001341834.1:p.Pro1531=
NM_001354906.1:c.4223C=	NP_001341835.1:p.Pro1408=
NM_000038.6:c.5072C= MANE Select	NP_000029.2:p.Pro1691=
NM_001127510.3:c.5072C=	NP_001120982.1:p.Pro1691=
NM_001127511.3:c.5018C=	NP_001120983.2:p.Pro1673=
NM_001354895.2:c.5072C=	NP_001341824.1:p.Pro1691=
NM_001354896.2:c.5126C=	NP_001341825.1:p.Pro1709=
NM_001354897.2:c.5102C=	NP_001341826.1:p.Pro1701=
NM_001354898.2:c.4997C=	NP_001341827.1:p.Pro1666=
NM_001354899.2:c.4988C=	NP_001341828.1:p.Pro1663=
NM_001354900.2:c.4949C=	NP_001341829.1:p.Pro1650=
NM_001354901.2:c.4895C=	NP_001341830.1:p.Pro1632=
NM_001354902.2:c.4799C=	NP_001341831.1:p.Pro1600=
NM_001354903.2:c.4769C=	NP_001341832.1:p.Pro1590=
NM_001354904.2:c.4694C=	NP_001341833.1:p.Pro1565=
NM_001354905.2:c.4592C=	NP_001341834.1:p.Pro1531=
NM_001354906.2:c.4223C=	NP_001341835.1:p.Pro1408=