Canonical Allele Identifier: CA2695204888

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838692_112838696del , CM000667.2:g.112838692_112838696del	GRCh38
NC_000005.9:g.112174389_112174393del , CM000667.1:g.112174389_112174393del	GRCh37
NC_000005.8:g.112202288_112202292del	NCBI36
NG_008481.4:g.151172_151176del , LRG_130:g.151172_151176del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2763_2767del	ENSP00000484935.2:n.2763_2767del
ENST00000504915.3:c.3152_3156del	ENSP00000473355.2:p.Asp1051AlafsTer13
ENST00000505350.2:c.*3104_*3108del	ENSP00000481752.1:n.*3104_*3108del
ENST00000507379.6:c.3044_3048del	ENSP00000423224.2:p.Asp1015AlafsTer13
ENST00000509732.6:c.3098_3102del	ENSP00000426541.2:p.Asp1033AlafsTer13
ENST00000512211.7:c.3098_3102del	ENSP00000423828.3:p.Asp1033AlafsTer13
ENST00000257430.9:c.3098_3102del MANE Select	ENSP00000257430.4:p.Asp1033AlafsTer13
ENST00000257430.8:c.3098_3102del	ENSP00000257430.4:p.Asp1033AlafsTer13
ENST00000502371.2:c.1451_1455del
ENST00000507379.5:c.3044_3048del	ENSP00000423224.1:p.Asp1015AlafsTer13
ENST00000508376.6:c.3098_3102del	ENSP00000427089.2:p.Asp1033AlafsTer13
ENST00000508624.5:c.*2420_*2424del	ENSP00000424265.1:n.*2420_*2424del
ENST00000512211.6:c.3098_3102del	ENSP00000423828.2:p.Asp1033AlafsTer13
ENST00000520401.1:c.230+9720_230+9724del
NM_000038.5:c.3098_3102del	NP_000029.2:p.Asp1033AlafsTer13
NM_001127510.2:c.3098_3102del	NP_001120982.1:p.Asp1033AlafsTer13
NM_001127511.2:c.3044_3048del	NP_001120983.2:p.Asp1015AlafsTer13
NM_001354895.1:c.3098_3102del	NP_001341824.1:p.Asp1033AlafsTer13
NM_001354896.1:c.3152_3156del	NP_001341825.1:p.Asp1051AlafsTer13
NM_001354897.1:c.3128_3132del	NP_001341826.1:p.Asp1043AlafsTer13
NM_001354898.1:c.3023_3027del	NP_001341827.1:p.Asp1008AlafsTer13
NM_001354899.1:c.3014_3018del	NP_001341828.1:p.Asp1005AlafsTer13
NM_001354900.1:c.2975_2979del	NP_001341829.1:p.Asp992AlafsTer13
NM_001354901.1:c.2921_2925del	NP_001341830.1:p.Asp974AlafsTer13
NM_001354902.1:c.2825_2829del	NP_001341831.1:p.Asp942AlafsTer13
NM_001354903.1:c.2795_2799del	NP_001341832.1:p.Asp932AlafsTer13
NM_001354904.1:c.2720_2724del	NP_001341833.1:p.Asp907AlafsTer13
NM_001354905.1:c.2618_2622del	NP_001341834.1:p.Asp873AlafsTer13
NM_001354906.1:c.2249_2253del	NP_001341835.1:p.Asp750AlafsTer13
NM_000038.6:c.3098_3102del MANE Select	NP_000029.2:p.Asp1033AlafsTer13
NM_001127510.3:c.3098_3102del	NP_001120982.1:p.Asp1033AlafsTer13
NM_001127511.3:c.3044_3048del	NP_001120983.2:p.Asp1015AlafsTer13
NM_001354895.2:c.3098_3102del	NP_001341824.1:p.Asp1033AlafsTer13
NM_001354896.2:c.3152_3156del	NP_001341825.1:p.Asp1051AlafsTer13
NM_001354897.2:c.3128_3132del	NP_001341826.1:p.Asp1043AlafsTer13
NM_001354898.2:c.3023_3027del	NP_001341827.1:p.Asp1008AlafsTer13
NM_001354899.2:c.3014_3018del	NP_001341828.1:p.Asp1005AlafsTer13
NM_001354900.2:c.2975_2979del	NP_001341829.1:p.Asp992AlafsTer13
NM_001354901.2:c.2921_2925del	NP_001341830.1:p.Asp974AlafsTer13
NM_001354902.2:c.2825_2829del	NP_001341831.1:p.Asp942AlafsTer13
NM_001354903.2:c.2795_2799del	NP_001341832.1:p.Asp932AlafsTer13
NM_001354904.2:c.2720_2724del	NP_001341833.1:p.Asp907AlafsTer13
NM_001354905.2:c.2618_2622del	NP_001341834.1:p.Asp873AlafsTer13
NM_001354906.2:c.2249_2253del	NP_001341835.1:p.Asp750AlafsTer13