Canonical Allele Identifier: CA658796577

Gene: APC

Linked Data

• ClinVar Variation Id: 537413
• ClinVar RCV Id: RCV002234011
• dbSNP Id: rs1554084704

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838709_112838710delinsCT , CM000667.2:g.112838709_112838710delinsCT	GRCh38
NC_000005.9:g.112174406_112174407delinsCT , CM000667.1:g.112174406_112174407delinsCT	GRCh37
NC_000005.8:g.112202305_112202306delinsCT	NCBI36
NG_008481.4:g.151189_151190delinsCT , LRG_130:g.151189_151190delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2780_2781delinsCT	ENSP00000484935.2:n.2780_2781delinsCT
ENST00000504915.3:c.3169_3170delinsCT	ENSP00000473355.2:p.Gly1057Leu
ENST00000505350.2:c.*3121_*3122delinsCT	ENSP00000481752.1:n.*3121_*3122delinsCT
ENST00000507379.6:c.3061_3062delinsCT	ENSP00000423224.2:p.Gly1021Leu
ENST00000509732.6:c.3115_3116delinsCT	ENSP00000426541.2:p.Gly1039Leu
ENST00000512211.7:c.3115_3116delinsCT	ENSP00000423828.3:p.Gly1039Leu
ENST00000257430.9:c.3115_3116delinsCT MANE Select	ENSP00000257430.4:p.Gly1039Leu
ENST00000257430.8:c.3115_3116delinsCT	ENSP00000257430.4:p.Gly1039Leu
ENST00000502371.2:c.1468_1469delinsCT
ENST00000507379.5:c.3061_3062delinsCT	ENSP00000423224.1:p.Gly1021Leu
ENST00000508376.6:c.3115_3116delinsCT	ENSP00000427089.2:p.Gly1039Leu
ENST00000508624.5:c.*2437_*2438delinsCT	ENSP00000424265.1:n.*2437_*2438delinsCT
ENST00000512211.6:c.3115_3116delinsCT	ENSP00000423828.2:p.Gly1039Leu
ENST00000520401.1:c.230+9737_230+9738delinsCT
NM_000038.5:c.3115_3116delinsCT	NP_000029.2:p.Gly1039Leu
NM_001127510.2:c.3115_3116delinsCT	NP_001120982.1:p.Gly1039Leu
NM_001127511.2:c.3061_3062delinsCT	NP_001120983.2:p.Gly1021Leu
NM_001354895.1:c.3115_3116delinsCT	NP_001341824.1:p.Gly1039Leu
NM_001354896.1:c.3169_3170delinsCT	NP_001341825.1:p.Gly1057Leu
NM_001354897.1:c.3145_3146delinsCT	NP_001341826.1:p.Gly1049Leu
NM_001354898.1:c.3040_3041delinsCT	NP_001341827.1:p.Gly1014Leu
NM_001354899.1:c.3031_3032delinsCT	NP_001341828.1:p.Gly1011Leu
NM_001354900.1:c.2992_2993delinsCT	NP_001341829.1:p.Gly998Leu
NM_001354901.1:c.2938_2939delinsCT	NP_001341830.1:p.Gly980Leu
NM_001354902.1:c.2842_2843delinsCT	NP_001341831.1:p.Gly948Leu
NM_001354903.1:c.2812_2813delinsCT	NP_001341832.1:p.Gly938Leu
NM_001354904.1:c.2737_2738delinsCT	NP_001341833.1:p.Gly913Leu
NM_001354905.1:c.2635_2636delinsCT	NP_001341834.1:p.Gly879Leu
NM_001354906.1:c.2266_2267delinsCT	NP_001341835.1:p.Gly756Leu
NM_000038.6:c.3115_3116delinsCT MANE Select	NP_000029.2:p.Gly1039Leu
NM_001127510.3:c.3115_3116delinsCT	NP_001120982.1:p.Gly1039Leu
NM_001127511.3:c.3061_3062delinsCT	NP_001120983.2:p.Gly1021Leu
NM_001354895.2:c.3115_3116delinsCT	NP_001341824.1:p.Gly1039Leu
NM_001354896.2:c.3169_3170delinsCT	NP_001341825.1:p.Gly1057Leu
NM_001354897.2:c.3145_3146delinsCT	NP_001341826.1:p.Gly1049Leu
NM_001354898.2:c.3040_3041delinsCT	NP_001341827.1:p.Gly1014Leu
NM_001354899.2:c.3031_3032delinsCT	NP_001341828.1:p.Gly1011Leu
NM_001354900.2:c.2992_2993delinsCT	NP_001341829.1:p.Gly998Leu
NM_001354901.2:c.2938_2939delinsCT	NP_001341830.1:p.Gly980Leu
NM_001354902.2:c.2842_2843delinsCT	NP_001341831.1:p.Gly948Leu
NM_001354903.2:c.2812_2813delinsCT	NP_001341832.1:p.Gly938Leu
NM_001354904.2:c.2737_2738delinsCT	NP_001341833.1:p.Gly913Leu
NM_001354905.2:c.2635_2636delinsCT	NP_001341834.1:p.Gly879Leu
NM_001354906.2:c.2266_2267delinsCT	NP_001341835.1:p.Gly756Leu