Canonical Allele Identifier: CA1573485627

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838638A= , CM000667.2:g.112838638A=	GRCh38
NC_000005.9:g.112174335A= , CM000667.1:g.112174335A=	GRCh37
NC_000005.8:g.112202234A=	NCBI36
NG_008481.4:g.151118A= , LRG_130:g.151118A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2709A=	ENSP00000484935.2:n.2709A=
ENST00000504915.3:c.3098A=	ENSP00000473355.2:p.Asp1033=
ENST00000505350.2:c.*3050A=	ENSP00000481752.1:n.*3050A=
ENST00000507379.6:c.2990A=	ENSP00000423224.2:p.Asp997=
ENST00000509732.6:c.3044A=	ENSP00000426541.2:p.Asp1015=
ENST00000512211.7:c.3044A=	ENSP00000423828.3:p.Asp1015=
ENST00000257430.9:c.3044A= MANE Select	ENSP00000257430.4:p.Asp1015=
ENST00000257430.8:c.3044A=	ENSP00000257430.4:p.Asp1015=
ENST00000502371.2:c.1397A=
ENST00000507379.5:c.2990A=	ENSP00000423224.1:p.Asp997=
ENST00000508376.6:c.3044A=	ENSP00000427089.2:p.Asp1015=
ENST00000508624.5:c.*2366A=	ENSP00000424265.1:n.*2366A=
ENST00000512211.6:c.3044A=	ENSP00000423828.2:p.Asp1015=
ENST00000520401.1:c.230+9666A=
NM_000038.5:c.3044A=	NP_000029.2:p.Asp1015=
NM_001127510.2:c.3044A=	NP_001120982.1:p.Asp1015=
NM_001127511.2:c.2990A=	NP_001120983.2:p.Asp997=
NM_001354895.1:c.3044A=	NP_001341824.1:p.Asp1015=
NM_001354896.1:c.3098A=	NP_001341825.1:p.Asp1033=
NM_001354897.1:c.3074A=	NP_001341826.1:p.Asp1025=
NM_001354898.1:c.2969A=	NP_001341827.1:p.Asp990=
NM_001354899.1:c.2960A=	NP_001341828.1:p.Asp987=
NM_001354900.1:c.2921A=	NP_001341829.1:p.Asp974=
NM_001354901.1:c.2867A=	NP_001341830.1:p.Asp956=
NM_001354902.1:c.2771A=	NP_001341831.1:p.Asp924=
NM_001354903.1:c.2741A=	NP_001341832.1:p.Asp914=
NM_001354904.1:c.2666A=	NP_001341833.1:p.Asp889=
NM_001354905.1:c.2564A=	NP_001341834.1:p.Asp855=
NM_001354906.1:c.2195A=	NP_001341835.1:p.Asp732=
NM_000038.6:c.3044A= MANE Select	NP_000029.2:p.Asp1015=
NM_001127510.3:c.3044A=	NP_001120982.1:p.Asp1015=
NM_001127511.3:c.2990A=	NP_001120983.2:p.Asp997=
NM_001354895.2:c.3044A=	NP_001341824.1:p.Asp1015=
NM_001354896.2:c.3098A=	NP_001341825.1:p.Asp1033=
NM_001354897.2:c.3074A=	NP_001341826.1:p.Asp1025=
NM_001354898.2:c.2969A=	NP_001341827.1:p.Asp990=
NM_001354899.2:c.2960A=	NP_001341828.1:p.Asp987=
NM_001354900.2:c.2921A=	NP_001341829.1:p.Asp974=
NM_001354901.2:c.2867A=	NP_001341830.1:p.Asp956=
NM_001354902.2:c.2771A=	NP_001341831.1:p.Asp924=
NM_001354903.2:c.2741A=	NP_001341832.1:p.Asp914=
NM_001354904.2:c.2666A=	NP_001341833.1:p.Asp889=
NM_001354905.2:c.2564A=	NP_001341834.1:p.Asp855=
NM_001354906.2:c.2195A=	NP_001341835.1:p.Asp732=