Canonical Allele Identifier: CA2582341627

Gene: APC

Linked Data

• ClinVar Variation Id: 2587011
• ClinVar RCV Id: RCV003339097

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843082_112843083insA , CM000667.2:g.112843082_112843083insA	GRCh38
NC_000005.9:g.112178779_112178780insA , CM000667.1:g.112178779_112178780insA	GRCh37
NC_000005.8:g.112206678_112206679insA	NCBI36
NG_008481.4:g.155562_155563insA , LRG_130:g.155562_155563insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7542_7543insA	ENSP00000473355.2:p.Ser2515IlefsTer14
ENST00000505350.2:c.*7494_*7495insA	ENSP00000481752.1:n.*7494_*7495insA
ENST00000507379.6:c.7434_7435insA	ENSP00000423224.2:p.Ser2479IlefsTer14
ENST00000509732.6:c.7488_7489insA	ENSP00000426541.2:p.Ser2497IlefsTer14
ENST00000512211.7:c.7488_7489insA	ENSP00000423828.3:p.Ser2497IlefsTer14
ENST00000257430.9:c.7488_7489insA MANE Select	ENSP00000257430.4:p.Ser2497IlefsTer14
ENST00000257430.8:c.7488_7489insA	ENSP00000257430.4:p.Ser2497IlefsTer14
ENST00000508376.6:c.7488_7489insA	ENSP00000427089.2:p.Ser2497IlefsTer14
ENST00000520401.1:c.231-13567_231-13566insA
NM_000038.5:c.7488_7489insA	NP_000029.2:p.Ser2497IlefsTer14
NM_001127510.2:c.7488_7489insA	NP_001120982.1:p.Ser2497IlefsTer14
NM_001127511.2:c.7434_7435insA	NP_001120983.2:p.Ser2479IlefsTer14
NM_001354895.1:c.7488_7489insA	NP_001341824.1:p.Ser2497IlefsTer14
NM_001354896.1:c.7542_7543insA	NP_001341825.1:p.Ser2515IlefsTer14
NM_001354897.1:c.7518_7519insA	NP_001341826.1:p.Ser2507IlefsTer14
NM_001354898.1:c.7413_7414insA	NP_001341827.1:p.Ser2472IlefsTer14
NM_001354899.1:c.7404_7405insA	NP_001341828.1:p.Ser2469IlefsTer14
NM_001354900.1:c.7365_7366insA	NP_001341829.1:p.Ser2456IlefsTer14
NM_001354901.1:c.7311_7312insA	NP_001341830.1:p.Ser2438IlefsTer14
NM_001354902.1:c.7215_7216insA	NP_001341831.1:p.Ser2406IlefsTer14
NM_001354903.1:c.7185_7186insA	NP_001341832.1:p.Ser2396IlefsTer14
NM_001354904.1:c.7110_7111insA	NP_001341833.1:p.Ser2371IlefsTer14
NM_001354905.1:c.7008_7009insA	NP_001341834.1:p.Ser2337IlefsTer14
NM_001354906.1:c.6639_6640insA	NP_001341835.1:p.Ser2214IlefsTer14
NM_000038.6:c.7488_7489insA MANE Select	NP_000029.2:p.Ser2497IlefsTer14
NM_001127510.3:c.7488_7489insA	NP_001120982.1:p.Ser2497IlefsTer14
NM_001127511.3:c.7434_7435insA	NP_001120983.2:p.Ser2479IlefsTer14
NM_001354895.2:c.7488_7489insA	NP_001341824.1:p.Ser2497IlefsTer14
NM_001354896.2:c.7542_7543insA	NP_001341825.1:p.Ser2515IlefsTer14
NM_001354897.2:c.7518_7519insA	NP_001341826.1:p.Ser2507IlefsTer14
NM_001354898.2:c.7413_7414insA	NP_001341827.1:p.Ser2472IlefsTer14
NM_001354899.2:c.7404_7405insA	NP_001341828.1:p.Ser2469IlefsTer14
NM_001354900.2:c.7365_7366insA	NP_001341829.1:p.Ser2456IlefsTer14
NM_001354901.2:c.7311_7312insA	NP_001341830.1:p.Ser2438IlefsTer14
NM_001354902.2:c.7215_7216insA	NP_001341831.1:p.Ser2406IlefsTer14
NM_001354903.2:c.7185_7186insA	NP_001341832.1:p.Ser2396IlefsTer14
NM_001354904.2:c.7110_7111insA	NP_001341833.1:p.Ser2371IlefsTer14
NM_001354905.2:c.7008_7009insA	NP_001341834.1:p.Ser2337IlefsTer14
NM_001354906.2:c.6639_6640insA	NP_001341835.1:p.Ser2214IlefsTer14