Canonical Allele Identifier: CA2573052388

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839037_112839038insG , CM000667.2:g.112839037_112839038insG	GRCh38
NC_000005.9:g.112174734_112174735insG , CM000667.1:g.112174734_112174735insG	GRCh37
NC_000005.8:g.112202633_112202634insG	NCBI36
NG_008481.4:g.151517_151518insG , LRG_130:g.151517_151518insG

Transcript Alleles

HGVS	Amino-acid Change
NM_000038.6:c.3443_3444insG MANE Select	NP_000029.2:p.Glu1149Ter
ENST00000257430.9:c.3443_3444insG MANE Select	ENSP00000257430.4:p.Glu1149Ter
NM_000038.5:c.3443_3444insG	NP_000029.2:p.Glu1149Ter
NM_001127510.2:c.3443_3444insG	NP_001120982.1:p.Glu1149Ter
NM_001127510.3:c.3443_3444insG	NP_001120982.1:p.Glu1149Ter
NM_001127511.2:c.3389_3390insG	NP_001120983.2:p.Glu1131Ter
NM_001127511.3:c.3389_3390insG	NP_001120983.2:p.Glu1131Ter
NM_001354895.1:c.3443_3444insG	NP_001341824.1:p.Glu1149Ter
NM_001354895.2:c.3443_3444insG	NP_001341824.1:p.Glu1149Ter
NM_001354896.1:c.3497_3498insG	NP_001341825.1:p.Glu1167Ter
NM_001354896.2:c.3497_3498insG	NP_001341825.1:p.Glu1167Ter
NM_001354897.1:c.3473_3474insG	NP_001341826.1:p.Glu1159Ter
NM_001354897.2:c.3473_3474insG	NP_001341826.1:p.Glu1159Ter
NM_001354898.1:c.3368_3369insG	NP_001341827.1:p.Glu1124Ter
NM_001354898.2:c.3368_3369insG	NP_001341827.1:p.Glu1124Ter
NM_001354899.1:c.3359_3360insG	NP_001341828.1:p.Glu1121Ter
NM_001354899.2:c.3359_3360insG	NP_001341828.1:p.Glu1121Ter
NM_001354900.1:c.3320_3321insG	NP_001341829.1:p.Glu1108Ter
NM_001354900.2:c.3320_3321insG	NP_001341829.1:p.Glu1108Ter
NM_001354901.1:c.3266_3267insG	NP_001341830.1:p.Glu1090Ter
NM_001354901.2:c.3266_3267insG	NP_001341830.1:p.Glu1090Ter
NM_001354902.1:c.3170_3171insG	NP_001341831.1:p.Glu1058Ter
NM_001354902.2:c.3170_3171insG	NP_001341831.1:p.Glu1058Ter
NM_001354903.1:c.3140_3141insG	NP_001341832.1:p.Glu1048Ter
NM_001354903.2:c.3140_3141insG	NP_001341832.1:p.Glu1048Ter
NM_001354904.1:c.3065_3066insG	NP_001341833.1:p.Glu1023Ter
NM_001354904.2:c.3065_3066insG	NP_001341833.1:p.Glu1023Ter
NM_001354905.1:c.2963_2964insG	NP_001341834.1:p.Glu989Ter
NM_001354905.2:c.2963_2964insG	NP_001341834.1:p.Glu989Ter
NM_001354906.1:c.2594_2595insG	NP_001341835.1:p.Glu866Ter
NM_001354906.2:c.2594_2595insG	NP_001341835.1:p.Glu866Ter
ENST00000257430.8:c.3443_3444insG	ENSP00000257430.4:p.Glu1149Ter
ENST00000502371.2:c.1796_1797insG
ENST00000502371.3:c.3108_3109insG	ENSP00000484935.2:n.3108_3109insG
ENST00000504915.3:c.3497_3498insG	ENSP00000473355.2:p.Glu1167Ter
ENST00000505350.2:c.*3449_*3450insG	ENSP00000481752.1:n.*3449_*3450insG
ENST00000507379.5:c.3389_3390insG	ENSP00000423224.1:p.Glu1131Ter
ENST00000507379.6:c.3389_3390insG	ENSP00000423224.2:p.Glu1131Ter
ENST00000508376.6:c.3443_3444insG	ENSP00000427089.2:p.Glu1149Ter
ENST00000508624.5:c.*2765_*2766insG	ENSP00000424265.1:n.*2765_*2766insG
ENST00000509732.6:c.3443_3444insG	ENSP00000426541.2:p.Glu1149Ter
ENST00000512211.6:c.3443_3444insG	ENSP00000423828.2:p.Glu1149Ter
ENST00000512211.7:c.3443_3444insG	ENSP00000423828.3:p.Glu1149Ter
ENST00000520401.1:c.230+10065_230+10066insG