Canonical Allele Identifier: CA16032890

Gene: APC

Linked Data

• ClinVar Variation Id: 919822
• ClinVar RCV Id: RCV001178232
• dbSNP Id: rs1765913275
• MyVariant Identifiers: chr5:g.112176579A>G (hg19) ; chr5:g.112840882A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840882A>G , CM000667.2:g.112840882A>G	GRCh38
NC_000005.9:g.112176579A>G , CM000667.1:g.112176579A>G	GRCh37
NC_000005.8:g.112204478A>G	NCBI36
NG_008481.4:g.153362A>G , LRG_130:g.153362A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.5342A>G	ENSP00000473355.2:p.Asn1781Ser
ENST00000505350.2:c.*5294A>G	ENSP00000481752.1:n.*5294A>G
ENST00000507379.6:c.5234A>G	ENSP00000423224.2:p.Asn1745Ser
ENST00000509732.6:c.5288A>G	ENSP00000426541.2:p.Asn1763Ser
ENST00000512211.7:c.5288A>G	ENSP00000423828.3:p.Asn1763Ser
ENST00000257430.9:c.5288A>G MANE Select	ENSP00000257430.4:p.Asn1763Ser
ENST00000257430.8:c.5288A>G	ENSP00000257430.4:p.Asn1763Ser
ENST00000508376.6:c.5288A>G	ENSP00000427089.2:p.Asn1763Ser
ENST00000508624.5:c.*4610A>G	ENSP00000424265.1:n.*4610A>G
ENST00000520401.1:c.230+11910A>G
NM_000038.5:c.5288A>G	NP_000029.2:p.Asn1763Ser
NM_001127510.2:c.5288A>G	NP_001120982.1:p.Asn1763Ser
NM_001127511.2:c.5234A>G	NP_001120983.2:p.Asn1745Ser
NM_001354895.1:c.5288A>G	NP_001341824.1:p.Asn1763Ser
NM_001354896.1:c.5342A>G	NP_001341825.1:p.Asn1781Ser
NM_001354897.1:c.5318A>G	NP_001341826.1:p.Asn1773Ser
NM_001354898.1:c.5213A>G	NP_001341827.1:p.Asn1738Ser
NM_001354899.1:c.5204A>G	NP_001341828.1:p.Asn1735Ser
NM_001354900.1:c.5165A>G	NP_001341829.1:p.Asn1722Ser
NM_001354901.1:c.5111A>G	NP_001341830.1:p.Asn1704Ser
NM_001354902.1:c.5015A>G	NP_001341831.1:p.Asn1672Ser
NM_001354903.1:c.4985A>G	NP_001341832.1:p.Asn1662Ser
NM_001354904.1:c.4910A>G	NP_001341833.1:p.Asn1637Ser
NM_001354905.1:c.4808A>G	NP_001341834.1:p.Asn1603Ser
NM_001354906.1:c.4439A>G	NP_001341835.1:p.Asn1480Ser
NM_000038.6:c.5288A>G MANE Select	NP_000029.2:p.Asn1763Ser
NM_001127510.3:c.5288A>G	NP_001120982.1:p.Asn1763Ser
NM_001127511.3:c.5234A>G	NP_001120983.2:p.Asn1745Ser
NM_001354895.2:c.5288A>G	NP_001341824.1:p.Asn1763Ser
NM_001354896.2:c.5342A>G	NP_001341825.1:p.Asn1781Ser
NM_001354897.2:c.5318A>G	NP_001341826.1:p.Asn1773Ser
NM_001354898.2:c.5213A>G	NP_001341827.1:p.Asn1738Ser
NM_001354899.2:c.5204A>G	NP_001341828.1:p.Asn1735Ser
NM_001354900.2:c.5165A>G	NP_001341829.1:p.Asn1722Ser
NM_001354901.2:c.5111A>G	NP_001341830.1:p.Asn1704Ser
NM_001354902.2:c.5015A>G	NP_001341831.1:p.Asn1672Ser
NM_001354903.2:c.4985A>G	NP_001341832.1:p.Asn1662Ser
NM_001354904.2:c.4910A>G	NP_001341833.1:p.Asn1637Ser
NM_001354905.2:c.4808A>G	NP_001341834.1:p.Asn1603Ser
NM_001354906.2:c.4439A>G	NP_001341835.1:p.Asn1480Ser