Canonical Allele Identifier: CA1573472992

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843300_112843306delinsGTTCATC , CM000667.2:g.112843300_112843306delinsGTTCATC	GRCh38
NC_000005.9:g.112178997_112179003delinsGTTCATC , CM000667.1:g.112178997_112179003delinsGTTCATC	GRCh37
NC_000005.8:g.112206896_112206902delinsGTTCATC	NCBI36
NG_008481.4:g.155780_155786delinsGTTCATC , LRG_130:g.155780_155786delinsGTTCATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7760_7766delinsGTTCATC	ENSP00000473355.2:p.Ser2587=
ENST00000505350.2:c.*7712_*7718delinsGTTCATC	ENSP00000481752.1:n.*7712_*7718delinsGTTCATC
ENST00000507379.6:c.7652_7658delinsGTTCATC	ENSP00000423224.2:p.Ser2551=
ENST00000509732.6:c.7706_7712delinsGTTCATC	ENSP00000426541.2:p.Ser2569=
ENST00000512211.7:c.7706_7712delinsGTTCATC	ENSP00000423828.3:p.Ser2569=
ENST00000257430.9:c.7706_7712delinsGTTCATC MANE Select	ENSP00000257430.4:p.Ser2569=
ENST00000257430.8:c.7706_7712delinsGTTCATC	ENSP00000257430.4:p.Ser2569=
ENST00000508376.6:c.7706_7712delinsGTTCATC	ENSP00000427089.2:p.Ser2569=
ENST00000520401.1:c.231-13349_231-13343delinsGTTCATC
NM_000038.5:c.7706_7712delinsGTTCATC	NP_000029.2:p.Ser2569=
NM_001127510.2:c.7706_7712delinsGTTCATC	NP_001120982.1:p.Ser2569=
NM_001127511.2:c.7652_7658delinsGTTCATC	NP_001120983.2:p.Ser2551=
NM_001354895.1:c.7706_7712delinsGTTCATC	NP_001341824.1:p.Ser2569=
NM_001354896.1:c.7760_7766delinsGTTCATC	NP_001341825.1:p.Ser2587=
NM_001354897.1:c.7736_7742delinsGTTCATC	NP_001341826.1:p.Ser2579=
NM_001354898.1:c.7631_7637delinsGTTCATC	NP_001341827.1:p.Ser2544=
NM_001354899.1:c.7622_7628delinsGTTCATC	NP_001341828.1:p.Ser2541=
NM_001354900.1:c.7583_7589delinsGTTCATC	NP_001341829.1:p.Ser2528=
NM_001354901.1:c.7529_7535delinsGTTCATC	NP_001341830.1:p.Ser2510=
NM_001354902.1:c.7433_7439delinsGTTCATC	NP_001341831.1:p.Ser2478=
NM_001354903.1:c.7403_7409delinsGTTCATC	NP_001341832.1:p.Ser2468=
NM_001354904.1:c.7328_7334delinsGTTCATC	NP_001341833.1:p.Ser2443=
NM_001354905.1:c.7226_7232delinsGTTCATC	NP_001341834.1:p.Ser2409=
NM_001354906.1:c.6857_6863delinsGTTCATC	NP_001341835.1:p.Ser2286=
NM_000038.6:c.7706_7712delinsGTTCATC MANE Select	NP_000029.2:p.Ser2569=
NM_001127510.3:c.7706_7712delinsGTTCATC	NP_001120982.1:p.Ser2569=
NM_001127511.3:c.7652_7658delinsGTTCATC	NP_001120983.2:p.Ser2551=
NM_001354895.2:c.7706_7712delinsGTTCATC	NP_001341824.1:p.Ser2569=
NM_001354896.2:c.7760_7766delinsGTTCATC	NP_001341825.1:p.Ser2587=
NM_001354897.2:c.7736_7742delinsGTTCATC	NP_001341826.1:p.Ser2579=
NM_001354898.2:c.7631_7637delinsGTTCATC	NP_001341827.1:p.Ser2544=
NM_001354899.2:c.7622_7628delinsGTTCATC	NP_001341828.1:p.Ser2541=
NM_001354900.2:c.7583_7589delinsGTTCATC	NP_001341829.1:p.Ser2528=
NM_001354901.2:c.7529_7535delinsGTTCATC	NP_001341830.1:p.Ser2510=
NM_001354902.2:c.7433_7439delinsGTTCATC	NP_001341831.1:p.Ser2478=
NM_001354903.2:c.7403_7409delinsGTTCATC	NP_001341832.1:p.Ser2468=
NM_001354904.2:c.7328_7334delinsGTTCATC	NP_001341833.1:p.Ser2443=
NM_001354905.2:c.7226_7232delinsGTTCATC	NP_001341834.1:p.Ser2409=
NM_001354906.2:c.6857_6863delinsGTTCATC	NP_001341835.1:p.Ser2286=