Canonical Allele Identifier: CA2709995022

Gene: APC

Linked Data

• dbSNP Id: rs2149997573

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843588_112843589del , CM000667.2:g.112843588_112843589del	GRCh38
NC_000005.9:g.112179285_112179286del , CM000667.1:g.112179285_112179286del	GRCh37
NC_000005.8:g.112207184_112207185del	NCBI36
NG_008481.4:g.156068_156069del , LRG_130:g.156068_156069del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8048_8049del	ENSP00000473355.2:p.Pro2683HisfsTer2
ENST00000505350.2:c.*8000_*8001del	ENSP00000481752.1:n.*8000_*8001del
ENST00000507379.6:c.7940_7941del	ENSP00000423224.2:p.Pro2647HisfsTer2
ENST00000509732.6:c.7994_7995del	ENSP00000426541.2:p.Pro2665HisfsTer2
ENST00000512211.7:c.7994_7995del	ENSP00000423828.3:p.Pro2665HisfsTer2
ENST00000257430.9:c.7994_7995del MANE Select	ENSP00000257430.4:p.Pro2665HisfsTer2
ENST00000257430.8:c.7994_7995del	ENSP00000257430.4:p.Pro2665HisfsTer2
ENST00000508376.6:c.7994_7995del	ENSP00000427089.2:p.Pro2665HisfsTer2
ENST00000520401.1:c.231-13061_231-13060del
NM_000038.5:c.7994_7995del	NP_000029.2:p.Pro2665HisfsTer2
NM_001127510.2:c.7994_7995del	NP_001120982.1:p.Pro2665HisfsTer2
NM_001127511.2:c.7940_7941del	NP_001120983.2:p.Pro2647HisfsTer2
NM_001354895.1:c.7994_7995del	NP_001341824.1:p.Pro2665HisfsTer2
NM_001354896.1:c.8048_8049del	NP_001341825.1:p.Pro2683HisfsTer2
NM_001354897.1:c.8024_8025del	NP_001341826.1:p.Pro2675HisfsTer2
NM_001354898.1:c.7919_7920del	NP_001341827.1:p.Pro2640HisfsTer2
NM_001354899.1:c.7910_7911del	NP_001341828.1:p.Pro2637HisfsTer2
NM_001354900.1:c.7871_7872del	NP_001341829.1:p.Pro2624HisfsTer2
NM_001354901.1:c.7817_7818del	NP_001341830.1:p.Pro2606HisfsTer2
NM_001354902.1:c.7721_7722del	NP_001341831.1:p.Pro2574HisfsTer2
NM_001354903.1:c.7691_7692del	NP_001341832.1:p.Pro2564HisfsTer2
NM_001354904.1:c.7616_7617del	NP_001341833.1:p.Pro2539HisfsTer2
NM_001354905.1:c.7514_7515del	NP_001341834.1:p.Pro2505HisfsTer2
NM_001354906.1:c.7145_7146del	NP_001341835.1:p.Pro2382HisfsTer2
NM_000038.6:c.7994_7995del MANE Select	NP_000029.2:p.Pro2665HisfsTer2
NM_001127510.3:c.7994_7995del	NP_001120982.1:p.Pro2665HisfsTer2
NM_001127511.3:c.7940_7941del	NP_001120983.2:p.Pro2647HisfsTer2
NM_001354895.2:c.7994_7995del	NP_001341824.1:p.Pro2665HisfsTer2
NM_001354896.2:c.8048_8049del	NP_001341825.1:p.Pro2683HisfsTer2
NM_001354897.2:c.8024_8025del	NP_001341826.1:p.Pro2675HisfsTer2
NM_001354898.2:c.7919_7920del	NP_001341827.1:p.Pro2640HisfsTer2
NM_001354899.2:c.7910_7911del	NP_001341828.1:p.Pro2637HisfsTer2
NM_001354900.2:c.7871_7872del	NP_001341829.1:p.Pro2624HisfsTer2
NM_001354901.2:c.7817_7818del	NP_001341830.1:p.Pro2606HisfsTer2
NM_001354902.2:c.7721_7722del	NP_001341831.1:p.Pro2574HisfsTer2
NM_001354903.2:c.7691_7692del	NP_001341832.1:p.Pro2564HisfsTer2
NM_001354904.2:c.7616_7617del	NP_001341833.1:p.Pro2539HisfsTer2
NM_001354905.2:c.7514_7515del	NP_001341834.1:p.Pro2505HisfsTer2
NM_001354906.2:c.7145_7146del	NP_001341835.1:p.Pro2382HisfsTer2