Canonical Allele Identifier: CA1573471268

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840336_112840341delinsCTGCCA , CM000667.2:g.112840336_112840341delinsCTGCCA	GRCh38
NC_000005.9:g.112176033_112176038delinsCTGCCA , CM000667.1:g.112176033_112176038delinsCTGCCA	GRCh37
NC_000005.8:g.112203932_112203937delinsCTGCCA	NCBI36
NG_008481.4:g.152816_152821delinsCTGCCA , LRG_130:g.152816_152821delinsCTGCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4796_4801delinsCTGCCA	ENSP00000473355.2:p.Ser1599=
ENST00000505350.2:c.*4748_*4753delinsCTGCCA	ENSP00000481752.1:n.*4748_*4753delinsCTGCCA
ENST00000507379.6:c.4688_4693delinsCTGCCA	ENSP00000423224.2:p.Ser1563=
ENST00000509732.6:c.4742_4747delinsCTGCCA	ENSP00000426541.2:p.Ser1581=
ENST00000512211.7:c.4742_4747delinsCTGCCA	ENSP00000423828.3:p.Ser1581=
ENST00000257430.9:c.4742_4747delinsCTGCCA MANE Select	ENSP00000257430.4:p.Ser1581=
ENST00000257430.8:c.4742_4747delinsCTGCCA	ENSP00000257430.4:p.Ser1581=
ENST00000508376.6:c.4742_4747delinsCTGCCA	ENSP00000427089.2:p.Ser1581=
ENST00000508624.5:c.*4064_*4069delinsCTGCCA	ENSP00000424265.1:n.*4064_*4069delinsCTGCCA
ENST00000520401.1:c.230+11364_230+11369delinsCTGCCA
NM_000038.5:c.4742_4747delinsCTGCCA	NP_000029.2:p.Ser1581=
NM_001127510.2:c.4742_4747delinsCTGCCA	NP_001120982.1:p.Ser1581=
NM_001127511.2:c.4688_4693delinsCTGCCA	NP_001120983.2:p.Ser1563=
NM_001354895.1:c.4742_4747delinsCTGCCA	NP_001341824.1:p.Ser1581=
NM_001354896.1:c.4796_4801delinsCTGCCA	NP_001341825.1:p.Ser1599=
NM_001354897.1:c.4772_4777delinsCTGCCA	NP_001341826.1:p.Ser1591=
NM_001354898.1:c.4667_4672delinsCTGCCA	NP_001341827.1:p.Ser1556=
NM_001354899.1:c.4658_4663delinsCTGCCA	NP_001341828.1:p.Ser1553=
NM_001354900.1:c.4619_4624delinsCTGCCA	NP_001341829.1:p.Ser1540=
NM_001354901.1:c.4565_4570delinsCTGCCA	NP_001341830.1:p.Ser1522=
NM_001354902.1:c.4469_4474delinsCTGCCA	NP_001341831.1:p.Ser1490=
NM_001354903.1:c.4439_4444delinsCTGCCA	NP_001341832.1:p.Ser1480=
NM_001354904.1:c.4364_4369delinsCTGCCA	NP_001341833.1:p.Ser1455=
NM_001354905.1:c.4262_4267delinsCTGCCA	NP_001341834.1:p.Ser1421=
NM_001354906.1:c.3893_3898delinsCTGCCA	NP_001341835.1:p.Ser1298=
NM_000038.6:c.4742_4747delinsCTGCCA MANE Select	NP_000029.2:p.Ser1581=
NM_001127510.3:c.4742_4747delinsCTGCCA	NP_001120982.1:p.Ser1581=
NM_001127511.3:c.4688_4693delinsCTGCCA	NP_001120983.2:p.Ser1563=
NM_001354895.2:c.4742_4747delinsCTGCCA	NP_001341824.1:p.Ser1581=
NM_001354896.2:c.4796_4801delinsCTGCCA	NP_001341825.1:p.Ser1599=
NM_001354897.2:c.4772_4777delinsCTGCCA	NP_001341826.1:p.Ser1591=
NM_001354898.2:c.4667_4672delinsCTGCCA	NP_001341827.1:p.Ser1556=
NM_001354899.2:c.4658_4663delinsCTGCCA	NP_001341828.1:p.Ser1553=
NM_001354900.2:c.4619_4624delinsCTGCCA	NP_001341829.1:p.Ser1540=
NM_001354901.2:c.4565_4570delinsCTGCCA	NP_001341830.1:p.Ser1522=
NM_001354902.2:c.4469_4474delinsCTGCCA	NP_001341831.1:p.Ser1490=
NM_001354903.2:c.4439_4444delinsCTGCCA	NP_001341832.1:p.Ser1480=
NM_001354904.2:c.4364_4369delinsCTGCCA	NP_001341833.1:p.Ser1455=
NM_001354905.2:c.4262_4267delinsCTGCCA	NP_001341834.1:p.Ser1421=
NM_001354906.2:c.3893_3898delinsCTGCCA	NP_001341835.1:p.Ser1298=