Canonical Allele Identifier: CA658760623

Gene: APC

Linked Data

• PubMed: PMID:16088911

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839526_112839530del , CM000667.2:g.112839526_112839530del	GRCh38
NC_000005.9:g.112175223_112175227del , CM000667.1:g.112175223_112175227del	GRCh37
NC_000005.8:g.112203122_112203126del	NCBI36
NG_008481.4:g.152006_152010del , LRG_130:g.152006_152010del

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.3597_3601del	ENSP00000484935.2:n.3597_3601del
ENST00000504915.3:c.3986_3990del	ENSP00000473355.2:p.Ile1329AsnfsTer2
ENST00000505350.2:c.*3938_*3942del	ENSP00000481752.1:n.*3938_*3942del
ENST00000507379.6:c.3878_3882del	ENSP00000423224.2:p.Ile1293AsnfsTer2
ENST00000509732.6:c.3932_3936del	ENSP00000426541.2:p.Ile1311AsnfsTer2
ENST00000512211.7:c.3932_3936del	ENSP00000423828.3:p.Ile1311AsnfsTer2
ENST00000257430.9:c.3932_3936del MANE Select	ENSP00000257430.4:p.Ile1311AsnfsTer2
ENST00000257430.8:c.3932_3936del	ENSP00000257430.4:p.Ile1311AsnfsTer2
ENST00000502371.2:c.2285_2289del
ENST00000508376.6:c.3932_3936del	ENSP00000427089.2:p.Ile1311AsnfsTer2
ENST00000508624.5:c.*3254_*3258del	ENSP00000424265.1:n.*3254_*3258del
ENST00000520401.1:c.230+10554_230+10558del
NM_000038.5:c.3932_3936del	NP_000029.2:p.Ile1311AsnfsTer2
NM_001127510.2:c.3932_3936del	NP_001120982.1:p.Ile1311AsnfsTer2
NM_001127511.2:c.3878_3882del	NP_001120983.2:p.Ile1293AsnfsTer2
NM_001354895.1:c.3932_3936del	NP_001341824.1:p.Ile1311AsnfsTer2
NM_001354896.1:c.3986_3990del	NP_001341825.1:p.Ile1329AsnfsTer2
NM_001354897.1:c.3962_3966del	NP_001341826.1:p.Ile1321AsnfsTer2
NM_001354898.1:c.3857_3861del	NP_001341827.1:p.Ile1286AsnfsTer2
NM_001354899.1:c.3848_3852del	NP_001341828.1:p.Ile1283AsnfsTer2
NM_001354900.1:c.3809_3813del	NP_001341829.1:p.Ile1270AsnfsTer2
NM_001354901.1:c.3755_3759del	NP_001341830.1:p.Ile1252AsnfsTer2
NM_001354902.1:c.3659_3663del	NP_001341831.1:p.Ile1220AsnfsTer2
NM_001354903.1:c.3629_3633del	NP_001341832.1:p.Ile1210AsnfsTer2
NM_001354904.1:c.3554_3558del	NP_001341833.1:p.Ile1185AsnfsTer2
NM_001354905.1:c.3452_3456del	NP_001341834.1:p.Ile1151AsnfsTer2
NM_001354906.1:c.3083_3087del	NP_001341835.1:p.Ile1028AsnfsTer2
NM_000038.6:c.3932_3936del MANE Select	NP_000029.2:p.Ile1311AsnfsTer2
NM_001127510.3:c.3932_3936del	NP_001120982.1:p.Ile1311AsnfsTer2
NM_001127511.3:c.3878_3882del	NP_001120983.2:p.Ile1293AsnfsTer2
NM_001354895.2:c.3932_3936del	NP_001341824.1:p.Ile1311AsnfsTer2
NM_001354896.2:c.3986_3990del	NP_001341825.1:p.Ile1329AsnfsTer2
NM_001354897.2:c.3962_3966del	NP_001341826.1:p.Ile1321AsnfsTer2
NM_001354898.2:c.3857_3861del	NP_001341827.1:p.Ile1286AsnfsTer2
NM_001354899.2:c.3848_3852del	NP_001341828.1:p.Ile1283AsnfsTer2
NM_001354900.2:c.3809_3813del	NP_001341829.1:p.Ile1270AsnfsTer2
NM_001354901.2:c.3755_3759del	NP_001341830.1:p.Ile1252AsnfsTer2
NM_001354902.2:c.3659_3663del	NP_001341831.1:p.Ile1220AsnfsTer2
NM_001354903.2:c.3629_3633del	NP_001341832.1:p.Ile1210AsnfsTer2
NM_001354904.2:c.3554_3558del	NP_001341833.1:p.Ile1185AsnfsTer2
NM_001354905.2:c.3452_3456del	NP_001341834.1:p.Ile1151AsnfsTer2
NM_001354906.2:c.3083_3087del	NP_001341835.1:p.Ile1028AsnfsTer2