Canonical Allele Identifier: CA16024507

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112162858C>A (hg19) ; chr5:g.112827161C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112827161C>A , CM000667.2:g.112827161C>A	GRCh38
NC_000005.9:g.112162858C>A , CM000667.1:g.112162858C>A	GRCh37
NC_000005.8:g.112190757C>A	NCBI36
NG_008481.4:g.139641C>A , LRG_130:g.139641C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1408+5170C>A	ENSP00000484935.2:n.1408+5170C>A
ENST00000504915.3:c.1516C>A	ENSP00000473355.2:p.Leu506Ile
ENST00000505084.2:n.1518C>A
ENST00000505350.2:c.*1468C>A	ENSP00000481752.1:n.*1468C>A
ENST00000507379.6:c.1408C>A	ENSP00000423224.2:p.Leu470Ile
ENST00000509732.6:c.1462C>A	ENSP00000426541.2:p.Leu488Ile
ENST00000512211.7:c.1462C>A	ENSP00000423828.3:p.Leu488Ile
ENST00000257430.9:c.1462C>A MANE Select	ENSP00000257430.4:p.Leu488Ile
ENST00000257430.8:c.1462C>A	ENSP00000257430.4:p.Leu488Ile
ENST00000502371.2:c.96+5170C>A
ENST00000504915.2:c.151C>A	ENSP00000473355.1:p.Leu51Ile
ENST00000507379.5:c.1408C>A	ENSP00000423224.1:p.Leu470Ile
ENST00000508376.6:c.1462C>A	ENSP00000427089.2:p.Leu488Ile
ENST00000508624.5:c.*784C>A	ENSP00000424265.1:n.*784C>A
ENST00000512211.6:c.1462C>A	ENSP00000423828.2:p.Leu488Ile
NM_000038.5:c.1462C>A	NP_000029.2:p.Leu488Ile
NM_001127510.2:c.1462C>A	NP_001120982.1:p.Leu488Ile
NM_001127511.2:c.1408C>A	NP_001120983.2:p.Leu470Ile
NM_001354895.1:c.1462C>A	NP_001341824.1:p.Leu488Ile
NM_001354896.1:c.1516C>A	NP_001341825.1:p.Leu506Ile
NM_001354897.1:c.1492C>A	NP_001341826.1:p.Leu498Ile
NM_001354898.1:c.1387C>A	NP_001341827.1:p.Leu463Ile
NM_001354899.1:c.1378C>A	NP_001341828.1:p.Leu460Ile
NM_001354900.1:c.1339C>A	NP_001341829.1:p.Leu447Ile
NM_001354901.1:c.1285C>A	NP_001341830.1:p.Leu429Ile
NM_001354902.1:c.1189C>A	NP_001341831.1:p.Leu397Ile
NM_001354903.1:c.1159C>A	NP_001341832.1:p.Leu387Ile
NM_001354904.1:c.1084C>A	NP_001341833.1:p.Leu362Ile
NM_001354905.1:c.982C>A	NP_001341834.1:p.Leu328Ile
NM_001354906.1:c.613C>A	NP_001341835.1:p.Leu205Ile
NM_000038.6:c.1462C>A MANE Select	NP_000029.2:p.Leu488Ile
NM_001127510.3:c.1462C>A	NP_001120982.1:p.Leu488Ile
NM_001127511.3:c.1408C>A	NP_001120983.2:p.Leu470Ile
NM_001354895.2:c.1462C>A	NP_001341824.1:p.Leu488Ile
NM_001354896.2:c.1516C>A	NP_001341825.1:p.Leu506Ile
NM_001354897.2:c.1492C>A	NP_001341826.1:p.Leu498Ile
NM_001354898.2:c.1387C>A	NP_001341827.1:p.Leu463Ile
NM_001354899.2:c.1378C>A	NP_001341828.1:p.Leu460Ile
NM_001354900.2:c.1339C>A	NP_001341829.1:p.Leu447Ile
NM_001354901.2:c.1285C>A	NP_001341830.1:p.Leu429Ile
NM_001354902.2:c.1189C>A	NP_001341831.1:p.Leu397Ile
NM_001354903.2:c.1159C>A	NP_001341832.1:p.Leu387Ile
NM_001354904.2:c.1084C>A	NP_001341833.1:p.Leu362Ile
NM_001354905.2:c.982C>A	NP_001341834.1:p.Leu328Ile
NM_001354906.2:c.613C>A	NP_001341835.1:p.Leu205Ile