Canonical Allele Identifier: CA1573471180

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835082G= , CM000667.2:g.112835082G=	GRCh38
NC_000005.9:g.112170779G= , CM000667.1:g.112170779G=	GRCh37
NC_000005.8:g.112198678G=	NCBI36
NG_008481.4:g.147562G= , LRG_130:g.147562G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1540G=	ENSP00000484935.2:n.1540G=
ENST00000504915.3:c.1929G=	ENSP00000473355.2:p.Gln643=
ENST00000505350.2:c.*1881G=	ENSP00000481752.1:n.*1881G=
ENST00000507379.6:c.1821G=	ENSP00000423224.2:p.Gln607=
ENST00000509732.6:c.1875G=	ENSP00000426541.2:p.Gln625=
ENST00000512211.7:c.1875G=	ENSP00000423828.3:p.Gln625=
ENST00000257430.9:c.1875G= MANE Select	ENSP00000257430.4:p.Gln625=
ENST00000257430.8:c.1875G=	ENSP00000257430.4:p.Gln625=
ENST00000502371.2:c.228G=
ENST00000504915.2:c.564G=	ENSP00000473355.1:p.Gln188=
ENST00000507379.5:c.1821G=	ENSP00000423224.1:p.Gln607=
ENST00000508376.6:c.1875G=	ENSP00000427089.2:p.Gln625=
ENST00000508624.5:c.*1197G=	ENSP00000424265.1:n.*1197G=
ENST00000512211.6:c.1875G=	ENSP00000423828.2:p.Gln625=
ENST00000520401.1:c.230+6110G=
NM_000038.5:c.1875G=	NP_000029.2:p.Gln625=
NM_001127510.2:c.1875G=	NP_001120982.1:p.Gln625=
NM_001127511.2:c.1821G=	NP_001120983.2:p.Gln607=
NM_001354895.1:c.1875G=	NP_001341824.1:p.Gln625=
NM_001354896.1:c.1929G=	NP_001341825.1:p.Gln643=
NM_001354897.1:c.1905G=	NP_001341826.1:p.Gln635=
NM_001354898.1:c.1800G=	NP_001341827.1:p.Gln600=
NM_001354899.1:c.1791G=	NP_001341828.1:p.Gln597=
NM_001354900.1:c.1752G=	NP_001341829.1:p.Gln584=
NM_001354901.1:c.1698G=	NP_001341830.1:p.Gln566=
NM_001354902.1:c.1602G=	NP_001341831.1:p.Gln534=
NM_001354903.1:c.1572G=	NP_001341832.1:p.Gln524=
NM_001354904.1:c.1497G=	NP_001341833.1:p.Gln499=
NM_001354905.1:c.1395G=	NP_001341834.1:p.Gln465=
NM_001354906.1:c.1026G=	NP_001341835.1:p.Gln342=
NM_000038.6:c.1875G= MANE Select	NP_000029.2:p.Gln625=
NM_001127510.3:c.1875G=	NP_001120982.1:p.Gln625=
NM_001127511.3:c.1821G=	NP_001120983.2:p.Gln607=
NM_001354895.2:c.1875G=	NP_001341824.1:p.Gln625=
NM_001354896.2:c.1929G=	NP_001341825.1:p.Gln643=
NM_001354897.2:c.1905G=	NP_001341826.1:p.Gln635=
NM_001354898.2:c.1800G=	NP_001341827.1:p.Gln600=
NM_001354899.2:c.1791G=	NP_001341828.1:p.Gln597=
NM_001354900.2:c.1752G=	NP_001341829.1:p.Gln584=
NM_001354901.2:c.1698G=	NP_001341830.1:p.Gln566=
NM_001354902.2:c.1602G=	NP_001341831.1:p.Gln534=
NM_001354903.2:c.1572G=	NP_001341832.1:p.Gln524=
NM_001354904.2:c.1497G=	NP_001341833.1:p.Gln499=
NM_001354905.2:c.1395G=	NP_001341834.1:p.Gln465=
NM_001354906.2:c.1026G=	NP_001341835.1:p.Gln342=