Canonical Allele Identifier: CA2697546210

Gene: APC

Linked Data

• ClinVar Variation Id: 2774878
• ClinVar RCV Id: RCV003586060

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838503_112838505del , CM000667.2:g.112838503_112838505del	GRCh38
NC_000005.9:g.112174200_112174202del , CM000667.1:g.112174200_112174202del	GRCh37
NC_000005.8:g.112202099_112202101del	NCBI36
NG_008481.4:g.150983_150985del , LRG_130:g.150983_150985del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.2574_2576del	ENSP00000484935.2:n.2574_2576del
ENST00000504915.3:c.2963_2965del	ENSP00000473355.2:p.Ser988_Asp989delinsAs...
ENST00000505350.2:c.*2915_*2917del	ENSP00000481752.1:n.*2915_*2917del
ENST00000507379.6:c.2855_2857del	ENSP00000423224.2:p.Ser952_Asp953delinsAs...
ENST00000509732.6:c.2909_2911del	ENSP00000426541.2:p.Ser970_Asp971delinsAs...
ENST00000512211.7:c.2909_2911del	ENSP00000423828.3:p.Ser970_Asp971delinsAs...
ENST00000257430.9:c.2909_2911del MANE Select	ENSP00000257430.4:p.Ser970_Asp971delinsAs...
ENST00000257430.8:c.2909_2911del	ENSP00000257430.4:p.Ser970_Asp971delinsAs...
ENST00000502371.2:c.1262_1264del
ENST00000507379.5:c.2855_2857del	ENSP00000423224.1:p.Ser952_Asp953delinsAs...
ENST00000508376.6:c.2909_2911del	ENSP00000427089.2:p.Ser970_Asp971delinsAs...
ENST00000508624.5:c.*2231_*2233del	ENSP00000424265.1:n.*2231_*2233del
ENST00000512211.6:c.2909_2911del	ENSP00000423828.2:p.Ser970_Asp971delinsAs...
ENST00000520401.1:c.230+9531_230+9533del
NM_000038.5:c.2909_2911del	NP_000029.2:p.Ser970_Asp971delinsAsn
NM_001127510.2:c.2909_2911del	NP_001120982.1:p.Ser970_Asp971delinsAsn
NM_001127511.2:c.2855_2857del	NP_001120983.2:p.Ser952_Asp953delinsAsn
NM_001354895.1:c.2909_2911del	NP_001341824.1:p.Ser970_Asp971delinsAsn
NM_001354896.1:c.2963_2965del	NP_001341825.1:p.Ser988_Asp989delinsAsn
NM_001354897.1:c.2939_2941del	NP_001341826.1:p.Ser980_Asp981delinsAsn
NM_001354898.1:c.2834_2836del	NP_001341827.1:p.Ser945_Asp946delinsAsn
NM_001354899.1:c.2825_2827del	NP_001341828.1:p.Ser942_Asp943delinsAsn
NM_001354900.1:c.2786_2788del	NP_001341829.1:p.Ser929_Asp930delinsAsn
NM_001354901.1:c.2732_2734del	NP_001341830.1:p.Ser911_Asp912delinsAsn
NM_001354902.1:c.2636_2638del	NP_001341831.1:p.Ser879_Asp880delinsAsn
NM_001354903.1:c.2606_2608del	NP_001341832.1:p.Ser869_Asp870delinsAsn
NM_001354904.1:c.2531_2533del	NP_001341833.1:p.Ser844_Asp845delinsAsn
NM_001354905.1:c.2429_2431del	NP_001341834.1:p.Ser810_Asp811delinsAsn
NM_001354906.1:c.2060_2062del	NP_001341835.1:p.Ser687_Asp688delinsAsn
NM_000038.6:c.2909_2911del MANE Select	NP_000029.2:p.Ser970_Asp971delinsAsn
NM_001127510.3:c.2909_2911del	NP_001120982.1:p.Ser970_Asp971delinsAsn
NM_001127511.3:c.2855_2857del	NP_001120983.2:p.Ser952_Asp953delinsAsn
NM_001354895.2:c.2909_2911del	NP_001341824.1:p.Ser970_Asp971delinsAsn
NM_001354896.2:c.2963_2965del	NP_001341825.1:p.Ser988_Asp989delinsAsn
NM_001354897.2:c.2939_2941del	NP_001341826.1:p.Ser980_Asp981delinsAsn
NM_001354898.2:c.2834_2836del	NP_001341827.1:p.Ser945_Asp946delinsAsn
NM_001354899.2:c.2825_2827del	NP_001341828.1:p.Ser942_Asp943delinsAsn
NM_001354900.2:c.2786_2788del	NP_001341829.1:p.Ser929_Asp930delinsAsn
NM_001354901.2:c.2732_2734del	NP_001341830.1:p.Ser911_Asp912delinsAsn
NM_001354902.2:c.2636_2638del	NP_001341831.1:p.Ser879_Asp880delinsAsn
NM_001354903.2:c.2606_2608del	NP_001341832.1:p.Ser869_Asp870delinsAsn
NM_001354904.2:c.2531_2533del	NP_001341833.1:p.Ser844_Asp845delinsAsn
NM_001354905.2:c.2429_2431del	NP_001341834.1:p.Ser810_Asp811delinsAsn
NM_001354906.2:c.2060_2062del	NP_001341835.1:p.Ser687_Asp688delinsAsn