Canonical Allele Identifier: CA2697546408

Gene: APC

Linked Data

• ClinVar Variation Id: 2733518
• ClinVar RCV Id: RCV003535123

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843383_112843384delinsTT , CM000667.2:g.112843383_112843384delinsTT	GRCh38
NC_000005.9:g.112179080_112179081delinsTT , CM000667.1:g.112179080_112179081delinsTT	GRCh37
NC_000005.8:g.112206979_112206980delinsTT	NCBI36
NG_008481.4:g.155863_155864delinsTT , LRG_130:g.155863_155864delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7843_7844delinsTT	ENSP00000473355.2:p.Gly2615Leu
ENST00000505350.2:c.*7795_*7796delinsTT	ENSP00000481752.1:n.*7795_*7796delinsTT
ENST00000507379.6:c.7735_7736delinsTT	ENSP00000423224.2:p.Gly2579Leu
ENST00000509732.6:c.7789_7790delinsTT	ENSP00000426541.2:p.Gly2597Leu
ENST00000512211.7:c.7789_7790delinsTT	ENSP00000423828.3:p.Gly2597Leu
ENST00000257430.9:c.7789_7790delinsTT MANE Select	ENSP00000257430.4:p.Gly2597Leu
ENST00000257430.8:c.7789_7790delinsTT	ENSP00000257430.4:p.Gly2597Leu
ENST00000508376.6:c.7789_7790delinsTT	ENSP00000427089.2:p.Gly2597Leu
ENST00000520401.1:c.231-13266_231-13265delinsTT
NM_000038.5:c.7789_7790delinsTT	NP_000029.2:p.Gly2597Leu
NM_001127510.2:c.7789_7790delinsTT	NP_001120982.1:p.Gly2597Leu
NM_001127511.2:c.7735_7736delinsTT	NP_001120983.2:p.Gly2579Leu
NM_001354895.1:c.7789_7790delinsTT	NP_001341824.1:p.Gly2597Leu
NM_001354896.1:c.7843_7844delinsTT	NP_001341825.1:p.Gly2615Leu
NM_001354897.1:c.7819_7820delinsTT	NP_001341826.1:p.Gly2607Leu
NM_001354898.1:c.7714_7715delinsTT	NP_001341827.1:p.Gly2572Leu
NM_001354899.1:c.7705_7706delinsTT	NP_001341828.1:p.Gly2569Leu
NM_001354900.1:c.7666_7667delinsTT	NP_001341829.1:p.Gly2556Leu
NM_001354901.1:c.7612_7613delinsTT	NP_001341830.1:p.Gly2538Leu
NM_001354902.1:c.7516_7517delinsTT	NP_001341831.1:p.Gly2506Leu
NM_001354903.1:c.7486_7487delinsTT	NP_001341832.1:p.Gly2496Leu
NM_001354904.1:c.7411_7412delinsTT	NP_001341833.1:p.Gly2471Leu
NM_001354905.1:c.7309_7310delinsTT	NP_001341834.1:p.Gly2437Leu
NM_001354906.1:c.6940_6941delinsTT	NP_001341835.1:p.Gly2314Leu
NM_000038.6:c.7789_7790delinsTT MANE Select	NP_000029.2:p.Gly2597Leu
NM_001127510.3:c.7789_7790delinsTT	NP_001120982.1:p.Gly2597Leu
NM_001127511.3:c.7735_7736delinsTT	NP_001120983.2:p.Gly2579Leu
NM_001354895.2:c.7789_7790delinsTT	NP_001341824.1:p.Gly2597Leu
NM_001354896.2:c.7843_7844delinsTT	NP_001341825.1:p.Gly2615Leu
NM_001354897.2:c.7819_7820delinsTT	NP_001341826.1:p.Gly2607Leu
NM_001354898.2:c.7714_7715delinsTT	NP_001341827.1:p.Gly2572Leu
NM_001354899.2:c.7705_7706delinsTT	NP_001341828.1:p.Gly2569Leu
NM_001354900.2:c.7666_7667delinsTT	NP_001341829.1:p.Gly2556Leu
NM_001354901.2:c.7612_7613delinsTT	NP_001341830.1:p.Gly2538Leu
NM_001354902.2:c.7516_7517delinsTT	NP_001341831.1:p.Gly2506Leu
NM_001354903.2:c.7486_7487delinsTT	NP_001341832.1:p.Gly2496Leu
NM_001354904.2:c.7411_7412delinsTT	NP_001341833.1:p.Gly2471Leu
NM_001354905.2:c.7309_7310delinsTT	NP_001341834.1:p.Gly2437Leu
NM_001354906.2:c.6940_6941delinsTT	NP_001341835.1:p.Gly2314Leu