Canonical Allele Identifier: CA913188208

Gene: APC

Linked Data

• ClinVar Variation Id: 918747
• ClinVar RCV Id: RCV001176480 ; RCV004032997 ; RCV003769880
• dbSNP Id: rs1765815215

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840560_112840561delinsAG , CM000667.2:g.112840560_112840561delinsAG	GRCh38
NC_000005.9:g.112176257_112176258delinsAG , CM000667.1:g.112176257_112176258delinsAG	GRCh37
NC_000005.8:g.112204156_112204157delinsAG	NCBI36
NG_008481.4:g.153040_153041delinsAG , LRG_130:g.153040_153041delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5020_5021delinsAG	ENSP00000473355.2:p.Ser1674=
ENST00000505350.2:c.*4972_*4973delinsAG	ENSP00000481752.1:n.*4972_*4973delinsAG
ENST00000507379.6:c.4912_4913delinsAG	ENSP00000423224.2:p.Ser1638=
ENST00000509732.6:c.4966_4967delinsAG	ENSP00000426541.2:p.Ser1656=
ENST00000512211.7:c.4966_4967delinsAG	ENSP00000423828.3:p.Ser1656=
ENST00000257430.9:c.4966_4967delinsAG MANE Select	ENSP00000257430.4:p.Ser1656=
ENST00000257430.8:c.4966_4967delinsAG	ENSP00000257430.4:p.Ser1656=
ENST00000508376.6:c.4966_4967delinsAG	ENSP00000427089.2:p.Ser1656=
ENST00000508624.5:c.*4288_*4289delinsAG	ENSP00000424265.1:n.*4288_*4289delinsAG
ENST00000520401.1:c.230+11588_230+11589delinsAG
NM_000038.5:c.4966_4967delinsAG	NP_000029.2:p.Ser1656=
NM_001127510.2:c.4966_4967delinsAG	NP_001120982.1:p.Ser1656=
NM_001127511.2:c.4912_4913delinsAG	NP_001120983.2:p.Ser1638=
NM_001354895.1:c.4966_4967delinsAG	NP_001341824.1:p.Ser1656=
NM_001354896.1:c.5020_5021delinsAG	NP_001341825.1:p.Ser1674=
NM_001354897.1:c.4996_4997delinsAG	NP_001341826.1:p.Ser1666=
NM_001354898.1:c.4891_4892delinsAG	NP_001341827.1:p.Ser1631=
NM_001354899.1:c.4882_4883delinsAG	NP_001341828.1:p.Ser1628=
NM_001354900.1:c.4843_4844delinsAG	NP_001341829.1:p.Ser1615=
NM_001354901.1:c.4789_4790delinsAG	NP_001341830.1:p.Ser1597=
NM_001354902.1:c.4693_4694delinsAG	NP_001341831.1:p.Ser1565=
NM_001354903.1:c.4663_4664delinsAG	NP_001341832.1:p.Ser1555=
NM_001354904.1:c.4588_4589delinsAG	NP_001341833.1:p.Ser1530=
NM_001354905.1:c.4486_4487delinsAG	NP_001341834.1:p.Ser1496=
NM_001354906.1:c.4117_4118delinsAG	NP_001341835.1:p.Ser1373=
NM_000038.6:c.4966_4967delinsAG MANE Select	NP_000029.2:p.Ser1656=
NM_001127510.3:c.4966_4967delinsAG	NP_001120982.1:p.Ser1656=
NM_001127511.3:c.4912_4913delinsAG	NP_001120983.2:p.Ser1638=
NM_001354895.2:c.4966_4967delinsAG	NP_001341824.1:p.Ser1656=
NM_001354896.2:c.5020_5021delinsAG	NP_001341825.1:p.Ser1674=
NM_001354897.2:c.4996_4997delinsAG	NP_001341826.1:p.Ser1666=
NM_001354898.2:c.4891_4892delinsAG	NP_001341827.1:p.Ser1631=
NM_001354899.2:c.4882_4883delinsAG	NP_001341828.1:p.Ser1628=
NM_001354900.2:c.4843_4844delinsAG	NP_001341829.1:p.Ser1615=
NM_001354901.2:c.4789_4790delinsAG	NP_001341830.1:p.Ser1597=
NM_001354902.2:c.4693_4694delinsAG	NP_001341831.1:p.Ser1565=
NM_001354903.2:c.4663_4664delinsAG	NP_001341832.1:p.Ser1555=
NM_001354904.2:c.4588_4589delinsAG	NP_001341833.1:p.Ser1530=
NM_001354905.2:c.4486_4487delinsAG	NP_001341834.1:p.Ser1496=
NM_001354906.2:c.4117_4118delinsAG	NP_001341835.1:p.Ser1373=