Canonical Allele Identifier: CA2582341313

Gene: APC

Linked Data

• ClinVar Variation Id: 2581174
• ClinVar RCV Id: RCV003331579

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840128_112843000del , CM000667.2:g.112840128_112843000del	GRCh38
NC_000005.9:g.112175825_112178697del , CM000667.1:g.112175825_112178697del	GRCh37
NC_000005.8:g.112203724_112206596del	NCBI36
NG_008481.4:g.152608_155480del , LRG_130:g.152608_155480del

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.4588_7460del	ENSP00000473355.2:p.Asp1530Ter
ENST00000505350.2:c.*4540_*7412del	ENSP00000481752.1:n.*4540_*7412del
ENST00000507379.6:c.4480_7352del	ENSP00000423224.2:p.Asp1494Ter
ENST00000509732.6:c.4534_7406del	ENSP00000426541.2:p.Asp1512Ter
ENST00000512211.7:c.4534_7406del	ENSP00000423828.3:p.Asp1512Ter
ENST00000257430.9:c.4534_7406del MANE Select	ENSP00000257430.4:p.Asp1512Ter
ENST00000257430.8:c.4534_7406del	ENSP00000257430.4:p.Asp1512Ter
ENST00000508376.6:c.4534_7406del	ENSP00000427089.2:p.Asp1512Ter
ENST00000520401.1:c.230+11156_231-13649del
NM_000038.5:c.4534_7406del	NP_000029.2:p.Asp1512Ter
NM_001127510.2:c.4534_7406del	NP_001120982.1:p.Asp1512Ter
NM_001127511.2:c.4480_7352del	NP_001120983.2:p.Asp1494Ter
NM_001354895.1:c.4534_7406del	NP_001341824.1:p.Asp1512Ter
NM_001354896.1:c.4588_7460del	NP_001341825.1:p.Asp1530Ter
NM_001354897.1:c.4564_7436del	NP_001341826.1:p.Asp1522Ter
NM_001354898.1:c.4459_7331del	NP_001341827.1:p.Asp1487Ter
NM_001354899.1:c.4450_7322del	NP_001341828.1:p.Asp1484Ter
NM_001354900.1:c.4411_7283del	NP_001341829.1:p.Asp1471Ter
NM_001354901.1:c.4357_7229del	NP_001341830.1:p.Asp1453Ter
NM_001354902.1:c.4261_7133del	NP_001341831.1:p.Asp1421Ter
NM_001354903.1:c.4231_7103del	NP_001341832.1:p.Asp1411Ter
NM_001354904.1:c.4156_7028del	NP_001341833.1:p.Asp1386Ter
NM_001354905.1:c.4054_6926del	NP_001341834.1:p.Asp1352Ter
NM_001354906.1:c.3685_6557del	NP_001341835.1:p.Asp1229Ter
NM_000038.6:c.4534_7406del MANE Select	NP_000029.2:p.Asp1512Ter
NM_001127510.3:c.4534_7406del	NP_001120982.1:p.Asp1512Ter
NM_001127511.3:c.4480_7352del	NP_001120983.2:p.Asp1494Ter
NM_001354895.2:c.4534_7406del	NP_001341824.1:p.Asp1512Ter
NM_001354896.2:c.4588_7460del	NP_001341825.1:p.Asp1530Ter
NM_001354897.2:c.4564_7436del	NP_001341826.1:p.Asp1522Ter
NM_001354898.2:c.4459_7331del	NP_001341827.1:p.Asp1487Ter
NM_001354899.2:c.4450_7322del	NP_001341828.1:p.Asp1484Ter
NM_001354900.2:c.4411_7283del	NP_001341829.1:p.Asp1471Ter
NM_001354901.2:c.4357_7229del	NP_001341830.1:p.Asp1453Ter
NM_001354902.2:c.4261_7133del	NP_001341831.1:p.Asp1421Ter
NM_001354903.2:c.4231_7103del	NP_001341832.1:p.Asp1411Ter
NM_001354904.2:c.4156_7028del	NP_001341833.1:p.Asp1386Ter
NM_001354905.2:c.4054_6926del	NP_001341834.1:p.Asp1352Ter
NM_001354906.2:c.3685_6557del	NP_001341835.1:p.Asp1229Ter