Canonical Allele Identifier: CA1573497140

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112821929_112821931delinsCTG , CM000667.2:g.112821929_112821931delinsCTG	GRCh38
NC_000005.9:g.112157626_112157628delinsCTG , CM000667.1:g.112157626_112157628delinsCTG	GRCh37
NC_000005.8:g.112185525_112185527delinsCTG	NCBI36
NG_008481.4:g.134409_134411delinsCTG , LRG_130:g.134409_134411delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1346_1348delinsCTG	ENSP00000484935.2:p.Ala449=
ENST00000504915.3:c.1346_1348delinsCTG	ENSP00000473355.2:p.Ala449=
ENST00000505084.2:n.1402_1404delinsCTG
ENST00000505350.2:c.*1352_*1354delinsCTG	ENSP00000481752.1:n.*1352_*1354delinsCTG
ENST00000507379.6:c.1292_1294delinsCTG	ENSP00000423224.2:p.Ala431=
ENST00000509732.6:c.1346_1348delinsCTG	ENSP00000426541.2:p.Ala449=
ENST00000512211.7:c.1346_1348delinsCTG	ENSP00000423828.3:p.Ala449=
ENST00000257430.9:c.1346_1348delinsCTG MANE Select	ENSP00000257430.4:p.Ala449=
ENST00000257430.8:c.1346_1348delinsCTG	ENSP00000257430.4:p.Ala449=
ENST00000502371.2:c.34_36delinsCTG
ENST00000507379.5:c.1292_1294delinsCTG	ENSP00000423224.1:p.Ala431=
ENST00000508376.6:c.1346_1348delinsCTG	ENSP00000427089.2:p.Ala449=
ENST00000508624.5:c.*668_*670delinsCTG	ENSP00000424265.1:n.*668_*670delinsCTG
ENST00000512211.6:c.1346_1348delinsCTG	ENSP00000423828.2:p.Ala449=
NM_000038.5:c.1346_1348delinsCTG	NP_000029.2:p.Ala449=
NM_001127510.2:c.1346_1348delinsCTG	NP_001120982.1:p.Ala449=
NM_001127511.2:c.1292_1294delinsCTG	NP_001120983.2:p.Ala431=
NM_001354895.1:c.1346_1348delinsCTG	NP_001341824.1:p.Ala449=
NM_001354896.1:c.1346_1348delinsCTG	NP_001341825.1:p.Ala449=
NM_001354897.1:c.1376_1378delinsCTG	NP_001341826.1:p.Ala459=
NM_001354898.1:c.1271_1273delinsCTG	NP_001341827.1:p.Ala424=
NM_001354899.1:c.1262_1264delinsCTG	NP_001341828.1:p.Ala421=
NM_001354900.1:c.1169_1171delinsCTG	NP_001341829.1:p.Ala390=
NM_001354901.1:c.1169_1171delinsCTG	NP_001341830.1:p.Ala390=
NM_001354902.1:c.1073_1075delinsCTG	NP_001341831.1:p.Ala358=
NM_001354903.1:c.1043_1045delinsCTG	NP_001341832.1:p.Ala348=
NM_001354904.1:c.968_970delinsCTG	NP_001341833.1:p.Ala323=
NM_001354905.1:c.866_868delinsCTG	NP_001341834.1:p.Ala289=
NM_001354906.1:c.497_499delinsCTG	NP_001341835.1:p.Ala166=
NM_000038.6:c.1346_1348delinsCTG MANE Select	NP_000029.2:p.Ala449=
NM_001127510.3:c.1346_1348delinsCTG	NP_001120982.1:p.Ala449=
NM_001127511.3:c.1292_1294delinsCTG	NP_001120983.2:p.Ala431=
NM_001354895.2:c.1346_1348delinsCTG	NP_001341824.1:p.Ala449=
NM_001354896.2:c.1346_1348delinsCTG	NP_001341825.1:p.Ala449=
NM_001354897.2:c.1376_1378delinsCTG	NP_001341826.1:p.Ala459=
NM_001354898.2:c.1271_1273delinsCTG	NP_001341827.1:p.Ala424=
NM_001354899.2:c.1262_1264delinsCTG	NP_001341828.1:p.Ala421=
NM_001354900.2:c.1169_1171delinsCTG	NP_001341829.1:p.Ala390=
NM_001354901.2:c.1169_1171delinsCTG	NP_001341830.1:p.Ala390=
NM_001354902.2:c.1073_1075delinsCTG	NP_001341831.1:p.Ala358=
NM_001354903.2:c.1043_1045delinsCTG	NP_001341832.1:p.Ala348=
NM_001354904.2:c.968_970delinsCTG	NP_001341833.1:p.Ala323=
NM_001354905.2:c.866_868delinsCTG	NP_001341834.1:p.Ala289=
NM_001354906.2:c.497_499delinsCTG	NP_001341835.1:p.Ala166=