Canonical Allele Identifier: CA2695204973

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839404_112839410delinsCTTTTCC , CM000667.2:g.112839404_112839410delinsCTTTTCC	GRCh38
NC_000005.9:g.112175101_112175107delinsCTTTTCC , CM000667.1:g.112175101_112175107delinsCTTTTCC	GRCh37
NC_000005.8:g.112203000_112203006delinsCTTTTCC	NCBI36
NG_008481.4:g.151884_151890delinsCTTTTCC , LRG_130:g.151884_151890delinsCTTTTCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.3475_3481delinsCTTTTCC	ENSP00000484935.2:n.3475_3481delinsCTTTTC...
ENST00000504915.3:c.3864_3870delinsCTTTTCC	ENSP00000473355.2:p.Cys1288=
ENST00000505350.2:c.*3816_*3822delinsCTTTTCC	ENSP00000481752.1:n.*3816_*3822delinsCTTT...
ENST00000507379.6:c.3756_3762delinsCTTTTCC	ENSP00000423224.2:p.Cys1252=
ENST00000509732.6:c.3810_3816delinsCTTTTCC	ENSP00000426541.2:p.Cys1270=
ENST00000512211.7:c.3810_3816delinsCTTTTCC	ENSP00000423828.3:p.Cys1270=
ENST00000257430.9:c.3810_3816delinsCTTTTCC MANE Select	ENSP00000257430.4:p.Cys1270=
ENST00000257430.8:c.3810_3816delinsCTTTTCC	ENSP00000257430.4:p.Cys1270=
ENST00000502371.2:c.2163_2169delinsCTTTTCC
ENST00000508376.6:c.3810_3816delinsCTTTTCC	ENSP00000427089.2:p.Cys1270=
ENST00000508624.5:c.*3132_*3138delinsCTTTTCC	ENSP00000424265.1:n.*3132_*3138delinsCTTT...
ENST00000512211.6:c.3810_3816delinsCTTTTCC	ENSP00000423828.2:p.Cys1270=
ENST00000520401.1:c.230+10432_230+10438delinsCTTTTCC
NM_000038.5:c.3810_3816delinsCTTTTCC	NP_000029.2:p.Cys1270=
NM_001127510.2:c.3810_3816delinsCTTTTCC	NP_001120982.1:p.Cys1270=
NM_001127511.2:c.3756_3762delinsCTTTTCC	NP_001120983.2:p.Cys1252=
NM_001354895.1:c.3810_3816delinsCTTTTCC	NP_001341824.1:p.Cys1270=
NM_001354896.1:c.3864_3870delinsCTTTTCC	NP_001341825.1:p.Cys1288=
NM_001354897.1:c.3840_3846delinsCTTTTCC	NP_001341826.1:p.Cys1280=
NM_001354898.1:c.3735_3741delinsCTTTTCC	NP_001341827.1:p.Cys1245=
NM_001354899.1:c.3726_3732delinsCTTTTCC	NP_001341828.1:p.Cys1242=
NM_001354900.1:c.3687_3693delinsCTTTTCC	NP_001341829.1:p.Cys1229=
NM_001354901.1:c.3633_3639delinsCTTTTCC	NP_001341830.1:p.Cys1211=
NM_001354902.1:c.3537_3543delinsCTTTTCC	NP_001341831.1:p.Cys1179=
NM_001354903.1:c.3507_3513delinsCTTTTCC	NP_001341832.1:p.Cys1169=
NM_001354904.1:c.3432_3438delinsCTTTTCC	NP_001341833.1:p.Cys1144=
NM_001354905.1:c.3330_3336delinsCTTTTCC	NP_001341834.1:p.Cys1110=
NM_001354906.1:c.2961_2967delinsCTTTTCC	NP_001341835.1:p.Cys987=
NM_000038.6:c.3810_3816delinsCTTTTCC MANE Select	NP_000029.2:p.Cys1270=
NM_001127510.3:c.3810_3816delinsCTTTTCC	NP_001120982.1:p.Cys1270=
NM_001127511.3:c.3756_3762delinsCTTTTCC	NP_001120983.2:p.Cys1252=
NM_001354895.2:c.3810_3816delinsCTTTTCC	NP_001341824.1:p.Cys1270=
NM_001354896.2:c.3864_3870delinsCTTTTCC	NP_001341825.1:p.Cys1288=
NM_001354897.2:c.3840_3846delinsCTTTTCC	NP_001341826.1:p.Cys1280=
NM_001354898.2:c.3735_3741delinsCTTTTCC	NP_001341827.1:p.Cys1245=
NM_001354899.2:c.3726_3732delinsCTTTTCC	NP_001341828.1:p.Cys1242=
NM_001354900.2:c.3687_3693delinsCTTTTCC	NP_001341829.1:p.Cys1229=
NM_001354901.2:c.3633_3639delinsCTTTTCC	NP_001341830.1:p.Cys1211=
NM_001354902.2:c.3537_3543delinsCTTTTCC	NP_001341831.1:p.Cys1179=
NM_001354903.2:c.3507_3513delinsCTTTTCC	NP_001341832.1:p.Cys1169=
NM_001354904.2:c.3432_3438delinsCTTTTCC	NP_001341833.1:p.Cys1144=
NM_001354905.2:c.3330_3336delinsCTTTTCC	NP_001341834.1:p.Cys1110=
NM_001354906.2:c.2961_2967delinsCTTTTCC	NP_001341835.1:p.Cys987=