Canonical Allele Identifier: CA891841971

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838672_112838673del , CM000667.2:g.112838672_112838673del	GRCh38
NC_000005.9:g.112174369_112174370del , CM000667.1:g.112174369_112174370del	GRCh37
NC_000005.8:g.112202268_112202269del	NCBI36
NG_008481.4:g.151152_151153del , LRG_130:g.151152_151153del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2743_2744del	ENSP00000484935.2:n.2743_2744del
ENST00000504915.3:c.3132_3133del	ENSP00000473355.2:p.Asn1044LysfsTer2
ENST00000505350.2:c.*3084_*3085del	ENSP00000481752.1:n.*3084_*3085del
ENST00000507379.6:c.3024_3025del	ENSP00000423224.2:p.Asn1008LysfsTer2
ENST00000509732.6:c.3078_3079del	ENSP00000426541.2:p.Asn1026LysfsTer2
ENST00000512211.7:c.3078_3079del	ENSP00000423828.3:p.Asn1026LysfsTer2
ENST00000257430.9:c.3078_3079del MANE Select	ENSP00000257430.4:p.Asn1026LysfsTer2
ENST00000257430.8:c.3078_3079del	ENSP00000257430.4:p.Asn1026LysfsTer2
ENST00000502371.2:c.1431_1432del
ENST00000507379.5:c.3024_3025del	ENSP00000423224.1:p.Asn1008LysfsTer2
ENST00000508376.6:c.3078_3079del	ENSP00000427089.2:p.Asn1026LysfsTer2
ENST00000508624.5:c.*2400_*2401del	ENSP00000424265.1:n.*2400_*2401del
ENST00000512211.6:c.3078_3079del	ENSP00000423828.2:p.Asn1026LysfsTer2
ENST00000520401.1:c.230+9700_230+9701del
NM_000038.5:c.3078_3079del	NP_000029.2:p.Asn1026LysfsTer2
NM_001127510.2:c.3078_3079del	NP_001120982.1:p.Asn1026LysfsTer2
NM_001127511.2:c.3024_3025del	NP_001120983.2:p.Asn1008LysfsTer2
NM_001354895.1:c.3078_3079del	NP_001341824.1:p.Asn1026LysfsTer2
NM_001354896.1:c.3132_3133del	NP_001341825.1:p.Asn1044LysfsTer2
NM_001354897.1:c.3108_3109del	NP_001341826.1:p.Asn1036LysfsTer2
NM_001354898.1:c.3003_3004del	NP_001341827.1:p.Asn1001LysfsTer2
NM_001354899.1:c.2994_2995del	NP_001341828.1:p.Asn998LysfsTer2
NM_001354900.1:c.2955_2956del	NP_001341829.1:p.Asn985LysfsTer2
NM_001354901.1:c.2901_2902del	NP_001341830.1:p.Asn967LysfsTer2
NM_001354902.1:c.2805_2806del	NP_001341831.1:p.Asn935LysfsTer2
NM_001354903.1:c.2775_2776del	NP_001341832.1:p.Asn925LysfsTer2
NM_001354904.1:c.2700_2701del	NP_001341833.1:p.Asn900LysfsTer2
NM_001354905.1:c.2598_2599del	NP_001341834.1:p.Asn866LysfsTer2
NM_001354906.1:c.2229_2230del	NP_001341835.1:p.Asn743LysfsTer2
NM_000038.6:c.3078_3079del MANE Select	NP_000029.2:p.Asn1026LysfsTer2
NM_001127510.3:c.3078_3079del	NP_001120982.1:p.Asn1026LysfsTer2
NM_001127511.3:c.3024_3025del	NP_001120983.2:p.Asn1008LysfsTer2
NM_001354895.2:c.3078_3079del	NP_001341824.1:p.Asn1026LysfsTer2
NM_001354896.2:c.3132_3133del	NP_001341825.1:p.Asn1044LysfsTer2
NM_001354897.2:c.3108_3109del	NP_001341826.1:p.Asn1036LysfsTer2
NM_001354898.2:c.3003_3004del	NP_001341827.1:p.Asn1001LysfsTer2
NM_001354899.2:c.2994_2995del	NP_001341828.1:p.Asn998LysfsTer2
NM_001354900.2:c.2955_2956del	NP_001341829.1:p.Asn985LysfsTer2
NM_001354901.2:c.2901_2902del	NP_001341830.1:p.Asn967LysfsTer2
NM_001354902.2:c.2805_2806del	NP_001341831.1:p.Asn935LysfsTer2
NM_001354903.2:c.2775_2776del	NP_001341832.1:p.Asn925LysfsTer2
NM_001354904.2:c.2700_2701del	NP_001341833.1:p.Asn900LysfsTer2
NM_001354905.2:c.2598_2599del	NP_001341834.1:p.Asn866LysfsTer2
NM_001354906.2:c.2229_2230del	NP_001341835.1:p.Asn743LysfsTer2