Canonical Allele Identifier: CA16032272

Gene: APC

Linked Data

• ClinVar Variation Id: 825363
• ClinVar RCV Id: RCV001023403 ; RCV001800936 ; RCV003649220
• dbSNP Id: rs1580655118
• MyVariant Identifiers: chr5:g.112176291A>G (hg19) ; chr5:g.112840594A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840594A>G , CM000667.2:g.112840594A>G	GRCh38
NC_000005.9:g.112176291A>G , CM000667.1:g.112176291A>G	GRCh37
NC_000005.8:g.112204190A>G	NCBI36
NG_008481.4:g.153074A>G , LRG_130:g.153074A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5054A>G	ENSP00000473355.2:p.Asn1685Ser
ENST00000505350.2:c.*5006A>G	ENSP00000481752.1:n.*5006A>G
ENST00000507379.6:c.4946A>G	ENSP00000423224.2:p.Asn1649Ser
ENST00000509732.6:c.5000A>G	ENSP00000426541.2:p.Asn1667Ser
ENST00000512211.7:c.5000A>G	ENSP00000423828.3:p.Asn1667Ser
ENST00000257430.9:c.5000A>G MANE Select	ENSP00000257430.4:p.Asn1667Ser
ENST00000257430.8:c.5000A>G	ENSP00000257430.4:p.Asn1667Ser
ENST00000508376.6:c.5000A>G	ENSP00000427089.2:p.Asn1667Ser
ENST00000508624.5:c.*4322A>G	ENSP00000424265.1:n.*4322A>G
ENST00000520401.1:c.230+11622A>G
NM_000038.5:c.5000A>G	NP_000029.2:p.Asn1667Ser
NM_001127510.2:c.5000A>G	NP_001120982.1:p.Asn1667Ser
NM_001127511.2:c.4946A>G	NP_001120983.2:p.Asn1649Ser
NM_001354895.1:c.5000A>G	NP_001341824.1:p.Asn1667Ser
NM_001354896.1:c.5054A>G	NP_001341825.1:p.Asn1685Ser
NM_001354897.1:c.5030A>G	NP_001341826.1:p.Asn1677Ser
NM_001354898.1:c.4925A>G	NP_001341827.1:p.Asn1642Ser
NM_001354899.1:c.4916A>G	NP_001341828.1:p.Asn1639Ser
NM_001354900.1:c.4877A>G	NP_001341829.1:p.Asn1626Ser
NM_001354901.1:c.4823A>G	NP_001341830.1:p.Asn1608Ser
NM_001354902.1:c.4727A>G	NP_001341831.1:p.Asn1576Ser
NM_001354903.1:c.4697A>G	NP_001341832.1:p.Asn1566Ser
NM_001354904.1:c.4622A>G	NP_001341833.1:p.Asn1541Ser
NM_001354905.1:c.4520A>G	NP_001341834.1:p.Asn1507Ser
NM_001354906.1:c.4151A>G	NP_001341835.1:p.Asn1384Ser
NM_000038.6:c.5000A>G MANE Select	NP_000029.2:p.Asn1667Ser
NM_001127510.3:c.5000A>G	NP_001120982.1:p.Asn1667Ser
NM_001127511.3:c.4946A>G	NP_001120983.2:p.Asn1649Ser
NM_001354895.2:c.5000A>G	NP_001341824.1:p.Asn1667Ser
NM_001354896.2:c.5054A>G	NP_001341825.1:p.Asn1685Ser
NM_001354897.2:c.5030A>G	NP_001341826.1:p.Asn1677Ser
NM_001354898.2:c.4925A>G	NP_001341827.1:p.Asn1642Ser
NM_001354899.2:c.4916A>G	NP_001341828.1:p.Asn1639Ser
NM_001354900.2:c.4877A>G	NP_001341829.1:p.Asn1626Ser
NM_001354901.2:c.4823A>G	NP_001341830.1:p.Asn1608Ser
NM_001354902.2:c.4727A>G	NP_001341831.1:p.Asn1576Ser
NM_001354903.2:c.4697A>G	NP_001341832.1:p.Asn1566Ser
NM_001354904.2:c.4622A>G	NP_001341833.1:p.Asn1541Ser
NM_001354905.2:c.4520A>G	NP_001341834.1:p.Asn1507Ser
NM_001354906.2:c.4151A>G	NP_001341835.1:p.Asn1384Ser