Canonical Allele Identifier: CA1573485693

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838646G= , CM000667.2:g.112838646G=	GRCh38
NC_000005.9:g.112174343G= , CM000667.1:g.112174343G=	GRCh37
NC_000005.8:g.112202242G=	NCBI36
NG_008481.4:g.151126G= , LRG_130:g.151126G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2717G=	ENSP00000484935.2:n.2717G=
ENST00000504915.3:c.3106G=	ENSP00000473355.2:p.Asp1036=
ENST00000505350.2:c.*3058G=	ENSP00000481752.1:n.*3058G=
ENST00000507379.6:c.2998G=	ENSP00000423224.2:p.Asp1000=
ENST00000509732.6:c.3052G=	ENSP00000426541.2:p.Asp1018=
ENST00000512211.7:c.3052G=	ENSP00000423828.3:p.Asp1018=
ENST00000257430.9:c.3052G= MANE Select	ENSP00000257430.4:p.Asp1018=
ENST00000257430.8:c.3052G=	ENSP00000257430.4:p.Asp1018=
ENST00000502371.2:c.1405G=
ENST00000507379.5:c.2998G=	ENSP00000423224.1:p.Asp1000=
ENST00000508376.6:c.3052G=	ENSP00000427089.2:p.Asp1018=
ENST00000508624.5:c.*2374G=	ENSP00000424265.1:n.*2374G=
ENST00000512211.6:c.3052G=	ENSP00000423828.2:p.Asp1018=
ENST00000520401.1:c.230+9674G=
NM_000038.5:c.3052G=	NP_000029.2:p.Asp1018=
NM_001127510.2:c.3052G=	NP_001120982.1:p.Asp1018=
NM_001127511.2:c.2998G=	NP_001120983.2:p.Asp1000=
NM_001354895.1:c.3052G=	NP_001341824.1:p.Asp1018=
NM_001354896.1:c.3106G=	NP_001341825.1:p.Asp1036=
NM_001354897.1:c.3082G=	NP_001341826.1:p.Asp1028=
NM_001354898.1:c.2977G=	NP_001341827.1:p.Asp993=
NM_001354899.1:c.2968G=	NP_001341828.1:p.Asp990=
NM_001354900.1:c.2929G=	NP_001341829.1:p.Asp977=
NM_001354901.1:c.2875G=	NP_001341830.1:p.Asp959=
NM_001354902.1:c.2779G=	NP_001341831.1:p.Asp927=
NM_001354903.1:c.2749G=	NP_001341832.1:p.Asp917=
NM_001354904.1:c.2674G=	NP_001341833.1:p.Asp892=
NM_001354905.1:c.2572G=	NP_001341834.1:p.Asp858=
NM_001354906.1:c.2203G=	NP_001341835.1:p.Asp735=
NM_000038.6:c.3052G= MANE Select	NP_000029.2:p.Asp1018=
NM_001127510.3:c.3052G=	NP_001120982.1:p.Asp1018=
NM_001127511.3:c.2998G=	NP_001120983.2:p.Asp1000=
NM_001354895.2:c.3052G=	NP_001341824.1:p.Asp1018=
NM_001354896.2:c.3106G=	NP_001341825.1:p.Asp1036=
NM_001354897.2:c.3082G=	NP_001341826.1:p.Asp1028=
NM_001354898.2:c.2977G=	NP_001341827.1:p.Asp993=
NM_001354899.2:c.2968G=	NP_001341828.1:p.Asp990=
NM_001354900.2:c.2929G=	NP_001341829.1:p.Asp977=
NM_001354901.2:c.2875G=	NP_001341830.1:p.Asp959=
NM_001354902.2:c.2779G=	NP_001341831.1:p.Asp927=
NM_001354903.2:c.2749G=	NP_001341832.1:p.Asp917=
NM_001354904.2:c.2674G=	NP_001341833.1:p.Asp892=
NM_001354905.2:c.2572G=	NP_001341834.1:p.Asp858=
NM_001354906.2:c.2203G=	NP_001341835.1:p.Asp735=