Canonical Allele Identifier: CA446208697
Gene: APC HGNC NCBI

Linked Data

dbSNP Id: rs2149927495
MyVariant Identifiers: chr5:g.112176214G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112840517G>C , CM000667.2:g.112840517G>C GRCh38
NC_000005.9:g.112176214G>C , CM000667.1:g.112176214G>C GRCh37
NC_000005.8:g.112204113G>C NCBI36
NG_008481.4:g.152997G>C , LRG_130:g.152997G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.4977G>C ENSP00000473355.2:p.Val1659=
ENST00000505350.2:c.*4929G>C ENSP00000481752.1:n.*4929G>C
ENST00000507379.6:c.4869G>C ENSP00000423224.2:p.Val1623=
ENST00000509732.6:c.4923G>C ENSP00000426541.2:p.Val1641=
ENST00000512211.7:c.4923G>C ENSP00000423828.3:p.Val1641=
ENST00000257430.9:c.4923G>C MANE Select ENSP00000257430.4:p.Val1641=
ENST00000257430.8:c.4923G>C ENSP00000257430.4:p.Val1641=
ENST00000508376.6:c.4923G>C ENSP00000427089.2:p.Val1641=
ENST00000508624.5:c.*4245G>C ENSP00000424265.1:n.*4245G>C
ENST00000520401.1:c.230+11545G>C
NM_000038.5:c.4923G>C NP_000029.2:p.Val1641=
NM_001127510.2:c.4923G>C NP_001120982.1:p.Val1641=
NM_001127511.2:c.4869G>C NP_001120983.2:p.Val1623=
NM_001354895.1:c.4923G>C NP_001341824.1:p.Val1641=
NM_001354896.1:c.4977G>C NP_001341825.1:p.Val1659=
NM_001354897.1:c.4953G>C NP_001341826.1:p.Val1651=
NM_001354898.1:c.4848G>C NP_001341827.1:p.Val1616=
NM_001354899.1:c.4839G>C NP_001341828.1:p.Val1613=
NM_001354900.1:c.4800G>C NP_001341829.1:p.Val1600=
NM_001354901.1:c.4746G>C NP_001341830.1:p.Val1582=
NM_001354902.1:c.4650G>C NP_001341831.1:p.Val1550=
NM_001354903.1:c.4620G>C NP_001341832.1:p.Val1540=
NM_001354904.1:c.4545G>C NP_001341833.1:p.Val1515=
NM_001354905.1:c.4443G>C NP_001341834.1:p.Val1481=
NM_001354906.1:c.4074G>C NP_001341835.1:p.Val1358=
NM_000038.6:c.4923G>C MANE Select NP_000029.2:p.Val1641=
NM_001127510.3:c.4923G>C NP_001120982.1:p.Val1641=
NM_001127511.3:c.4869G>C NP_001120983.2:p.Val1623=
NM_001354895.2:c.4923G>C NP_001341824.1:p.Val1641=
NM_001354896.2:c.4977G>C NP_001341825.1:p.Val1659=
NM_001354897.2:c.4953G>C NP_001341826.1:p.Val1651=
NM_001354898.2:c.4848G>C NP_001341827.1:p.Val1616=
NM_001354899.2:c.4839G>C NP_001341828.1:p.Val1613=
NM_001354900.2:c.4800G>C NP_001341829.1:p.Val1600=
NM_001354901.2:c.4746G>C NP_001341830.1:p.Val1582=
NM_001354902.2:c.4650G>C NP_001341831.1:p.Val1550=
NM_001354903.2:c.4620G>C NP_001341832.1:p.Val1540=
NM_001354904.2:c.4545G>C NP_001341833.1:p.Val1515=
NM_001354905.2:c.4443G>C NP_001341834.1:p.Val1481=
NM_001354906.2:c.4074G>C NP_001341835.1:p.Val1358=