Canonical Allele Identifier: CA16031547

Gene: APC

Linked Data

• ClinVar Variation Id: 433664
• ClinVar RCV Id: RCV000504432 ; RCV002231173
• dbSNP Id: rs1392778905
• COSMIC: COSM33818
• MyVariant Identifiers: chr5:g.112175951G>T (hg19) ; chr5:g.112840254G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840254G>T , CM000667.2:g.112840254G>T	GRCh38
NC_000005.9:g.112175951G>T , CM000667.1:g.112175951G>T	GRCh37
NC_000005.8:g.112203850G>T	NCBI36
NG_008481.4:g.152734G>T , LRG_130:g.152734G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4714G>T	ENSP00000473355.2:p.Glu1572Ter
ENST00000505350.2:c.*4666G>T	ENSP00000481752.1:n.*4666G>T
ENST00000507379.6:c.4606G>T	ENSP00000423224.2:p.Glu1536Ter
ENST00000509732.6:c.4660G>T	ENSP00000426541.2:p.Glu1554Ter
ENST00000512211.7:c.4660G>T	ENSP00000423828.3:p.Glu1554Ter
ENST00000257430.9:c.4660G>T MANE Select	ENSP00000257430.4:p.Glu1554Ter
ENST00000257430.8:c.4660G>T	ENSP00000257430.4:p.Glu1554Ter
ENST00000508376.6:c.4660G>T	ENSP00000427089.2:p.Glu1554Ter
ENST00000508624.5:c.*3982G>T	ENSP00000424265.1:n.*3982G>T
ENST00000520401.1:c.230+11282G>T
NM_000038.5:c.4660G>T	NP_000029.2:p.Glu1554Ter
NM_001127510.2:c.4660G>T	NP_001120982.1:p.Glu1554Ter
NM_001127511.2:c.4606G>T	NP_001120983.2:p.Glu1536Ter
NM_001354895.1:c.4660G>T	NP_001341824.1:p.Glu1554Ter
NM_001354896.1:c.4714G>T	NP_001341825.1:p.Glu1572Ter
NM_001354897.1:c.4690G>T	NP_001341826.1:p.Glu1564Ter
NM_001354898.1:c.4585G>T	NP_001341827.1:p.Glu1529Ter
NM_001354899.1:c.4576G>T	NP_001341828.1:p.Glu1526Ter
NM_001354900.1:c.4537G>T	NP_001341829.1:p.Glu1513Ter
NM_001354901.1:c.4483G>T	NP_001341830.1:p.Glu1495Ter
NM_001354902.1:c.4387G>T	NP_001341831.1:p.Glu1463Ter
NM_001354903.1:c.4357G>T	NP_001341832.1:p.Glu1453Ter
NM_001354904.1:c.4282G>T	NP_001341833.1:p.Glu1428Ter
NM_001354905.1:c.4180G>T	NP_001341834.1:p.Glu1394Ter
NM_001354906.1:c.3811G>T	NP_001341835.1:p.Glu1271Ter
NM_000038.6:c.4660G>T MANE Select	NP_000029.2:p.Glu1554Ter
NM_001127510.3:c.4660G>T	NP_001120982.1:p.Glu1554Ter
NM_001127511.3:c.4606G>T	NP_001120983.2:p.Glu1536Ter
NM_001354895.2:c.4660G>T	NP_001341824.1:p.Glu1554Ter
NM_001354896.2:c.4714G>T	NP_001341825.1:p.Glu1572Ter
NM_001354897.2:c.4690G>T	NP_001341826.1:p.Glu1564Ter
NM_001354898.2:c.4585G>T	NP_001341827.1:p.Glu1529Ter
NM_001354899.2:c.4576G>T	NP_001341828.1:p.Glu1526Ter
NM_001354900.2:c.4537G>T	NP_001341829.1:p.Glu1513Ter
NM_001354901.2:c.4483G>T	NP_001341830.1:p.Glu1495Ter
NM_001354902.2:c.4387G>T	NP_001341831.1:p.Glu1463Ter
NM_001354903.2:c.4357G>T	NP_001341832.1:p.Glu1453Ter
NM_001354904.2:c.4282G>T	NP_001341833.1:p.Glu1428Ter
NM_001354905.2:c.4180G>T	NP_001341834.1:p.Glu1394Ter
NM_001354906.2:c.3811G>T	NP_001341835.1:p.Glu1271Ter