Canonical Allele Identifier: CA16025286

Gene: APC

Linked Data

• ClinVar Variation Id: 490227
• ClinVar RCV Id: RCV000583720 ; RCV001755969 ; RCV003744589
• dbSNP Id: rs370955311
• gnomAD v4: 5-112835018-C-T
• MyVariant Identifiers: chr5:g.112170715C>T (hg19) ; chr5:g.112835018C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835018C>T , CM000667.2:g.112835018C>T	GRCh38
NC_000005.9:g.112170715C>T , CM000667.1:g.112170715C>T	GRCh37
NC_000005.8:g.112198614C>T	NCBI36
NG_008481.4:g.147498C>T , LRG_130:g.147498C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1476C>T	ENSP00000484935.2:n.1476C>T
ENST00000504915.3:c.1865C>T	ENSP00000473355.2:p.Ala622Val
ENST00000505350.2:c.*1817C>T	ENSP00000481752.1:n.*1817C>T
ENST00000507379.6:c.1757C>T	ENSP00000423224.2:p.Ala586Val
ENST00000509732.6:c.1811C>T	ENSP00000426541.2:p.Ala604Val
ENST00000512211.7:c.1811C>T	ENSP00000423828.3:p.Ala604Val
ENST00000257430.9:c.1811C>T MANE Select	ENSP00000257430.4:p.Ala604Val
ENST00000257430.8:c.1811C>T	ENSP00000257430.4:p.Ala604Val
ENST00000502371.2:c.164C>T
ENST00000504915.2:c.500C>T	ENSP00000473355.1:p.Ala167Val
ENST00000507379.5:c.1757C>T	ENSP00000423224.1:p.Ala586Val
ENST00000508376.6:c.1811C>T	ENSP00000427089.2:p.Ala604Val
ENST00000508624.5:c.*1133C>T	ENSP00000424265.1:n.*1133C>T
ENST00000512211.6:c.1811C>T	ENSP00000423828.2:p.Ala604Val
ENST00000520401.1:c.230+6046C>T
NM_000038.5:c.1811C>T	NP_000029.2:p.Ala604Val
NM_001127510.2:c.1811C>T	NP_001120982.1:p.Ala604Val
NM_001127511.2:c.1757C>T	NP_001120983.2:p.Ala586Val
NM_001354895.1:c.1811C>T	NP_001341824.1:p.Ala604Val
NM_001354896.1:c.1865C>T	NP_001341825.1:p.Ala622Val
NM_001354897.1:c.1841C>T	NP_001341826.1:p.Ala614Val
NM_001354898.1:c.1736C>T	NP_001341827.1:p.Ala579Val
NM_001354899.1:c.1727C>T	NP_001341828.1:p.Ala576Val
NM_001354900.1:c.1688C>T	NP_001341829.1:p.Ala563Val
NM_001354901.1:c.1634C>T	NP_001341830.1:p.Ala545Val
NM_001354902.1:c.1538C>T	NP_001341831.1:p.Ala513Val
NM_001354903.1:c.1508C>T	NP_001341832.1:p.Ala503Val
NM_001354904.1:c.1433C>T	NP_001341833.1:p.Ala478Val
NM_001354905.1:c.1331C>T	NP_001341834.1:p.Ala444Val
NM_001354906.1:c.962C>T	NP_001341835.1:p.Ala321Val
NM_000038.6:c.1811C>T MANE Select	NP_000029.2:p.Ala604Val
NM_001127510.3:c.1811C>T	NP_001120982.1:p.Ala604Val
NM_001127511.3:c.1757C>T	NP_001120983.2:p.Ala586Val
NM_001354895.2:c.1811C>T	NP_001341824.1:p.Ala604Val
NM_001354896.2:c.1865C>T	NP_001341825.1:p.Ala622Val
NM_001354897.2:c.1841C>T	NP_001341826.1:p.Ala614Val
NM_001354898.2:c.1736C>T	NP_001341827.1:p.Ala579Val
NM_001354899.2:c.1727C>T	NP_001341828.1:p.Ala576Val
NM_001354900.2:c.1688C>T	NP_001341829.1:p.Ala563Val
NM_001354901.2:c.1634C>T	NP_001341830.1:p.Ala545Val
NM_001354902.2:c.1538C>T	NP_001341831.1:p.Ala513Val
NM_001354903.2:c.1508C>T	NP_001341832.1:p.Ala503Val
NM_001354904.2:c.1433C>T	NP_001341833.1:p.Ala478Val
NM_001354905.2:c.1331C>T	NP_001341834.1:p.Ala444Val
NM_001354906.2:c.962C>T	NP_001341835.1:p.Ala321Val