Canonical Allele Identifier: CA1573490721

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839420_112839423delinsTCAT , CM000667.2:g.112839420_112839423delinsTCAT	GRCh38
NC_000005.9:g.112175117_112175120delinsTCAT , CM000667.1:g.112175117_112175120delinsTCAT	GRCh37
NC_000005.8:g.112203016_112203019delinsTCAT	NCBI36
NG_008481.4:g.151900_151903delinsTCAT , LRG_130:g.151900_151903delinsTCAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.3491_3494delinsTCAT	ENSP00000484935.2:n.3491_3494delinsTCAT
ENST00000504915.3:c.3880_3883delinsTCAT	ENSP00000473355.2:p.Ser1294=
ENST00000505350.2:c.*3832_*3835delinsTCAT	ENSP00000481752.1:n.*3832_*3835delinsTCAT...
ENST00000507379.6:c.3772_3775delinsTCAT	ENSP00000423224.2:p.Ser1258=
ENST00000509732.6:c.3826_3829delinsTCAT	ENSP00000426541.2:p.Ser1276=
ENST00000512211.7:c.3826_3829delinsTCAT	ENSP00000423828.3:p.Ser1276=
ENST00000257430.9:c.3826_3829delinsTCAT MANE Select	ENSP00000257430.4:p.Ser1276=
ENST00000257430.8:c.3826_3829delinsTCAT	ENSP00000257430.4:p.Ser1276=
ENST00000502371.2:c.2179_2182delinsTCAT
ENST00000508376.6:c.3826_3829delinsTCAT	ENSP00000427089.2:p.Ser1276=
ENST00000508624.5:c.*3148_*3151delinsTCAT	ENSP00000424265.1:n.*3148_*3151delinsTCAT...
ENST00000512211.6:c.3826_3829delinsTCAT	ENSP00000423828.2:p.Ser1276=
ENST00000520401.1:c.230+10448_230+10451delinsTCAT
NM_000038.5:c.3826_3829delinsTCAT	NP_000029.2:p.Ser1276=
NM_001127510.2:c.3826_3829delinsTCAT	NP_001120982.1:p.Ser1276=
NM_001127511.2:c.3772_3775delinsTCAT	NP_001120983.2:p.Ser1258=
NM_001354895.1:c.3826_3829delinsTCAT	NP_001341824.1:p.Ser1276=
NM_001354896.1:c.3880_3883delinsTCAT	NP_001341825.1:p.Ser1294=
NM_001354897.1:c.3856_3859delinsTCAT	NP_001341826.1:p.Ser1286=
NM_001354898.1:c.3751_3754delinsTCAT	NP_001341827.1:p.Ser1251=
NM_001354899.1:c.3742_3745delinsTCAT	NP_001341828.1:p.Ser1248=
NM_001354900.1:c.3703_3706delinsTCAT	NP_001341829.1:p.Ser1235=
NM_001354901.1:c.3649_3652delinsTCAT	NP_001341830.1:p.Ser1217=
NM_001354902.1:c.3553_3556delinsTCAT	NP_001341831.1:p.Ser1185=
NM_001354903.1:c.3523_3526delinsTCAT	NP_001341832.1:p.Ser1175=
NM_001354904.1:c.3448_3451delinsTCAT	NP_001341833.1:p.Ser1150=
NM_001354905.1:c.3346_3349delinsTCAT	NP_001341834.1:p.Ser1116=
NM_001354906.1:c.2977_2980delinsTCAT	NP_001341835.1:p.Ser993=
NM_000038.6:c.3826_3829delinsTCAT MANE Select	NP_000029.2:p.Ser1276=
NM_001127510.3:c.3826_3829delinsTCAT	NP_001120982.1:p.Ser1276=
NM_001127511.3:c.3772_3775delinsTCAT	NP_001120983.2:p.Ser1258=
NM_001354895.2:c.3826_3829delinsTCAT	NP_001341824.1:p.Ser1276=
NM_001354896.2:c.3880_3883delinsTCAT	NP_001341825.1:p.Ser1294=
NM_001354897.2:c.3856_3859delinsTCAT	NP_001341826.1:p.Ser1286=
NM_001354898.2:c.3751_3754delinsTCAT	NP_001341827.1:p.Ser1251=
NM_001354899.2:c.3742_3745delinsTCAT	NP_001341828.1:p.Ser1248=
NM_001354900.2:c.3703_3706delinsTCAT	NP_001341829.1:p.Ser1235=
NM_001354901.2:c.3649_3652delinsTCAT	NP_001341830.1:p.Ser1217=
NM_001354902.2:c.3553_3556delinsTCAT	NP_001341831.1:p.Ser1185=
NM_001354903.2:c.3523_3526delinsTCAT	NP_001341832.1:p.Ser1175=
NM_001354904.2:c.3448_3451delinsTCAT	NP_001341833.1:p.Ser1150=
NM_001354905.2:c.3346_3349delinsTCAT	NP_001341834.1:p.Ser1116=
NM_001354906.2:c.2977_2980delinsTCAT	NP_001341835.1:p.Ser993=