Canonical Allele Identifier: CA16032887

Gene: APC

Linked Data

• ClinVar Variation Id: 944980
• ClinVar RCV Id: RCV003650711
• dbSNP Id: rs1440736149
• MyVariant Identifiers: chr5:g.112176578A>G (hg19) ; chr5:g.112840881A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840881A>G , CM000667.2:g.112840881A>G	GRCh38
NC_000005.9:g.112176578A>G , CM000667.1:g.112176578A>G	GRCh37
NC_000005.8:g.112204477A>G	NCBI36
NG_008481.4:g.153361A>G , LRG_130:g.153361A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.5341A>G	ENSP00000473355.2:p.Asn1781Asp
ENST00000505350.2:c.*5293A>G	ENSP00000481752.1:n.*5293A>G
ENST00000507379.6:c.5233A>G	ENSP00000423224.2:p.Asn1745Asp
ENST00000509732.6:c.5287A>G	ENSP00000426541.2:p.Asn1763Asp
ENST00000512211.7:c.5287A>G	ENSP00000423828.3:p.Asn1763Asp
ENST00000257430.9:c.5287A>G MANE Select	ENSP00000257430.4:p.Asn1763Asp
ENST00000257430.8:c.5287A>G	ENSP00000257430.4:p.Asn1763Asp
ENST00000508376.6:c.5287A>G	ENSP00000427089.2:p.Asn1763Asp
ENST00000508624.5:c.*4609A>G	ENSP00000424265.1:n.*4609A>G
ENST00000520401.1:c.230+11909A>G
NM_000038.5:c.5287A>G	NP_000029.2:p.Asn1763Asp
NM_001127510.2:c.5287A>G	NP_001120982.1:p.Asn1763Asp
NM_001127511.2:c.5233A>G	NP_001120983.2:p.Asn1745Asp
NM_001354895.1:c.5287A>G	NP_001341824.1:p.Asn1763Asp
NM_001354896.1:c.5341A>G	NP_001341825.1:p.Asn1781Asp
NM_001354897.1:c.5317A>G	NP_001341826.1:p.Asn1773Asp
NM_001354898.1:c.5212A>G	NP_001341827.1:p.Asn1738Asp
NM_001354899.1:c.5203A>G	NP_001341828.1:p.Asn1735Asp
NM_001354900.1:c.5164A>G	NP_001341829.1:p.Asn1722Asp
NM_001354901.1:c.5110A>G	NP_001341830.1:p.Asn1704Asp
NM_001354902.1:c.5014A>G	NP_001341831.1:p.Asn1672Asp
NM_001354903.1:c.4984A>G	NP_001341832.1:p.Asn1662Asp
NM_001354904.1:c.4909A>G	NP_001341833.1:p.Asn1637Asp
NM_001354905.1:c.4807A>G	NP_001341834.1:p.Asn1603Asp
NM_001354906.1:c.4438A>G	NP_001341835.1:p.Asn1480Asp
NM_000038.6:c.5287A>G MANE Select	NP_000029.2:p.Asn1763Asp
NM_001127510.3:c.5287A>G	NP_001120982.1:p.Asn1763Asp
NM_001127511.3:c.5233A>G	NP_001120983.2:p.Asn1745Asp
NM_001354895.2:c.5287A>G	NP_001341824.1:p.Asn1763Asp
NM_001354896.2:c.5341A>G	NP_001341825.1:p.Asn1781Asp
NM_001354897.2:c.5317A>G	NP_001341826.1:p.Asn1773Asp
NM_001354898.2:c.5212A>G	NP_001341827.1:p.Asn1738Asp
NM_001354899.2:c.5203A>G	NP_001341828.1:p.Asn1735Asp
NM_001354900.2:c.5164A>G	NP_001341829.1:p.Asn1722Asp
NM_001354901.2:c.5110A>G	NP_001341830.1:p.Asn1704Asp
NM_001354902.2:c.5014A>G	NP_001341831.1:p.Asn1672Asp
NM_001354903.2:c.4984A>G	NP_001341832.1:p.Asn1662Asp
NM_001354904.2:c.4909A>G	NP_001341833.1:p.Asn1637Asp
NM_001354905.2:c.4807A>G	NP_001341834.1:p.Asn1603Asp
NM_001354906.2:c.4438A>G	NP_001341835.1:p.Asn1480Asp