Canonical Allele Identifier: CA2695204884

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838657dup , CM000667.2:g.112838657dup	GRCh38
NC_000005.9:g.112174354dup , CM000667.1:g.112174354dup	GRCh37
NC_000005.8:g.112202253dup	NCBI36
NG_008481.4:g.151137dup , LRG_130:g.151137dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2728dup	ENSP00000484935.2:n.2728dup
ENST00000504915.3:c.3117dup	ENSP00000473355.2:p.Asp1040ArgfsTer7
ENST00000505350.2:c.*3069dup	ENSP00000481752.1:n.*3069dup
ENST00000507379.6:c.3009dup	ENSP00000423224.2:p.Asp1004ArgfsTer7
ENST00000509732.6:c.3063dup	ENSP00000426541.2:p.Asp1022ArgfsTer7
ENST00000512211.7:c.3063dup	ENSP00000423828.3:p.Asp1022ArgfsTer7
ENST00000257430.9:c.3063dup MANE Select	ENSP00000257430.4:p.Asp1022ArgfsTer7
ENST00000257430.8:c.3063dup	ENSP00000257430.4:p.Asp1022ArgfsTer7
ENST00000502371.2:c.1416dup
ENST00000507379.5:c.3009dup	ENSP00000423224.1:p.Asp1004ArgfsTer7
ENST00000508376.6:c.3063dup	ENSP00000427089.2:p.Asp1022ArgfsTer7
ENST00000508624.5:c.*2385dup	ENSP00000424265.1:n.*2385dup
ENST00000512211.6:c.3063dup	ENSP00000423828.2:p.Asp1022ArgfsTer7
ENST00000520401.1:c.230+9685dup
NM_000038.5:c.3063dup	NP_000029.2:p.Asp1022ArgfsTer7
NM_001127510.2:c.3063dup	NP_001120982.1:p.Asp1022ArgfsTer7
NM_001127511.2:c.3009dup	NP_001120983.2:p.Asp1004ArgfsTer7
NM_001354895.1:c.3063dup	NP_001341824.1:p.Asp1022ArgfsTer7
NM_001354896.1:c.3117dup	NP_001341825.1:p.Asp1040ArgfsTer7
NM_001354897.1:c.3093dup	NP_001341826.1:p.Asp1032ArgfsTer7
NM_001354898.1:c.2988dup	NP_001341827.1:p.Asp997ArgfsTer7
NM_001354899.1:c.2979dup	NP_001341828.1:p.Asp994ArgfsTer7
NM_001354900.1:c.2940dup	NP_001341829.1:p.Asp981ArgfsTer7
NM_001354901.1:c.2886dup	NP_001341830.1:p.Asp963ArgfsTer7
NM_001354902.1:c.2790dup	NP_001341831.1:p.Asp931ArgfsTer7
NM_001354903.1:c.2760dup	NP_001341832.1:p.Asp921ArgfsTer7
NM_001354904.1:c.2685dup	NP_001341833.1:p.Asp896ArgfsTer7
NM_001354905.1:c.2583dup	NP_001341834.1:p.Asp862ArgfsTer7
NM_001354906.1:c.2214dup	NP_001341835.1:p.Asp739ArgfsTer7
NM_000038.6:c.3063dup MANE Select	NP_000029.2:p.Asp1022ArgfsTer7
NM_001127510.3:c.3063dup	NP_001120982.1:p.Asp1022ArgfsTer7
NM_001127511.3:c.3009dup	NP_001120983.2:p.Asp1004ArgfsTer7
NM_001354895.2:c.3063dup	NP_001341824.1:p.Asp1022ArgfsTer7
NM_001354896.2:c.3117dup	NP_001341825.1:p.Asp1040ArgfsTer7
NM_001354897.2:c.3093dup	NP_001341826.1:p.Asp1032ArgfsTer7
NM_001354898.2:c.2988dup	NP_001341827.1:p.Asp997ArgfsTer7
NM_001354899.2:c.2979dup	NP_001341828.1:p.Asp994ArgfsTer7
NM_001354900.2:c.2940dup	NP_001341829.1:p.Asp981ArgfsTer7
NM_001354901.2:c.2886dup	NP_001341830.1:p.Asp963ArgfsTer7
NM_001354902.2:c.2790dup	NP_001341831.1:p.Asp931ArgfsTer7
NM_001354903.2:c.2760dup	NP_001341832.1:p.Asp921ArgfsTer7
NM_001354904.2:c.2685dup	NP_001341833.1:p.Asp896ArgfsTer7
NM_001354905.2:c.2583dup	NP_001341834.1:p.Asp862ArgfsTer7
NM_001354906.2:c.2214dup	NP_001341835.1:p.Asp739ArgfsTer7