Canonical Allele Identifier: CA645543551

Gene: APC

Linked Data

• COSMIC: COSM4169384

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838675_112838676delinsGAC , CM000667.2:g.112838675_112838676delinsGAC	GRCh38
NC_000005.9:g.112174372_112174373delinsGAC , CM000667.1:g.112174372_112174373delinsGAC	GRCh37
NC_000005.8:g.112202271_112202272delinsGAC	NCBI36
NG_008481.4:g.151155_151156delinsGAC , LRG_130:g.151155_151156delinsGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2746_2747delinsGAC	ENSP00000484935.2:n.2746_2747delinsGAC
ENST00000504915.3:c.3135_3136delinsGAC	ENSP00000473355.2:p.Tyr1045Ter
ENST00000505350.2:c.*3087_*3088delinsGAC	ENSP00000481752.1:n.*3087_*3088delinsGAC
ENST00000507379.6:c.3027_3028delinsGAC	ENSP00000423224.2:p.Tyr1009Ter
ENST00000509732.6:c.3081_3082delinsGAC	ENSP00000426541.2:p.Tyr1027Ter
ENST00000512211.7:c.3081_3082delinsGAC	ENSP00000423828.3:p.Tyr1027Ter
ENST00000257430.9:c.3081_3082delinsGAC MANE Select	ENSP00000257430.4:p.Tyr1027Ter
ENST00000257430.8:c.3081_3082delinsGAC	ENSP00000257430.4:p.Tyr1027Ter
ENST00000502371.2:c.1434_1435delinsGAC
ENST00000507379.5:c.3027_3028delinsGAC	ENSP00000423224.1:p.Tyr1009Ter
ENST00000508376.6:c.3081_3082delinsGAC	ENSP00000427089.2:p.Tyr1027Ter
ENST00000508624.5:c.*2403_*2404delinsGAC	ENSP00000424265.1:n.*2403_*2404delinsGAC
ENST00000512211.6:c.3081_3082delinsGAC	ENSP00000423828.2:p.Tyr1027Ter
ENST00000520401.1:c.230+9703_230+9704delinsGAC
NM_000038.5:c.3081_3082delinsGAC	NP_000029.2:p.Tyr1027Ter
NM_001127510.2:c.3081_3082delinsGAC	NP_001120982.1:p.Tyr1027Ter
NM_001127511.2:c.3027_3028delinsGAC	NP_001120983.2:p.Tyr1009Ter
NM_001354895.1:c.3081_3082delinsGAC	NP_001341824.1:p.Tyr1027Ter
NM_001354896.1:c.3135_3136delinsGAC	NP_001341825.1:p.Tyr1045Ter
NM_001354897.1:c.3111_3112delinsGAC	NP_001341826.1:p.Tyr1037Ter
NM_001354898.1:c.3006_3007delinsGAC	NP_001341827.1:p.Tyr1002Ter
NM_001354899.1:c.2997_2998delinsGAC	NP_001341828.1:p.Tyr999Ter
NM_001354900.1:c.2958_2959delinsGAC	NP_001341829.1:p.Tyr986Ter
NM_001354901.1:c.2904_2905delinsGAC	NP_001341830.1:p.Tyr968Ter
NM_001354902.1:c.2808_2809delinsGAC	NP_001341831.1:p.Tyr936Ter
NM_001354903.1:c.2778_2779delinsGAC	NP_001341832.1:p.Tyr926Ter
NM_001354904.1:c.2703_2704delinsGAC	NP_001341833.1:p.Tyr901Ter
NM_001354905.1:c.2601_2602delinsGAC	NP_001341834.1:p.Tyr867Ter
NM_001354906.1:c.2232_2233delinsGAC	NP_001341835.1:p.Tyr744Ter
NM_000038.6:c.3081_3082delinsGAC MANE Select	NP_000029.2:p.Tyr1027Ter
NM_001127510.3:c.3081_3082delinsGAC	NP_001120982.1:p.Tyr1027Ter
NM_001127511.3:c.3027_3028delinsGAC	NP_001120983.2:p.Tyr1009Ter
NM_001354895.2:c.3081_3082delinsGAC	NP_001341824.1:p.Tyr1027Ter
NM_001354896.2:c.3135_3136delinsGAC	NP_001341825.1:p.Tyr1045Ter
NM_001354897.2:c.3111_3112delinsGAC	NP_001341826.1:p.Tyr1037Ter
NM_001354898.2:c.3006_3007delinsGAC	NP_001341827.1:p.Tyr1002Ter
NM_001354899.2:c.2997_2998delinsGAC	NP_001341828.1:p.Tyr999Ter
NM_001354900.2:c.2958_2959delinsGAC	NP_001341829.1:p.Tyr986Ter
NM_001354901.2:c.2904_2905delinsGAC	NP_001341830.1:p.Tyr968Ter
NM_001354902.2:c.2808_2809delinsGAC	NP_001341831.1:p.Tyr936Ter
NM_001354903.2:c.2778_2779delinsGAC	NP_001341832.1:p.Tyr926Ter
NM_001354904.2:c.2703_2704delinsGAC	NP_001341833.1:p.Tyr901Ter
NM_001354905.2:c.2601_2602delinsGAC	NP_001341834.1:p.Tyr867Ter
NM_001354906.2:c.2232_2233delinsGAC	NP_001341835.1:p.Tyr744Ter