Canonical Allele Identifier: CA010884
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41509
dbSNP Id: rs141576417

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112780865C>G , CM000667.2:g.112780865C>G GRCh38
NC_000005.9:g.112116562C>G , CM000667.1:g.112116562C>G GRCh37
NC_000005.8:g.112144461C>G NCBI36
NG_008481.4:g.93345C>G , LRG_130:g.93345C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000502371.3:c.607C>G ENSP00000484935.2:p.Gln203Glu
ENST00000504915.3:c.607C>G ENSP00000473355.2:p.Gln203Glu
ENST00000505084.2:n.663C>G
ENST00000505350.2:c.*613C>G ENSP00000481752.1:n.*613C>G
ENST00000507379.6:c.637C>G ENSP00000423224.2:p.Gln213Glu
ENST00000509732.6:c.607C>G ENSP00000426541.2:p.Gln203Glu
ENST00000512211.7:c.607C>G ENSP00000423828.3:p.Gln203Glu
ENST00000257430.9:c.607C>G MANE Select ENSP00000257430.4:p.Gln203Glu
ENST00000257430.8:c.607C>G ENSP00000257430.4:p.Gln203Glu
ENST00000507379.5:c.637C>G ENSP00000423224.1:p.Gln213Glu
ENST00000508376.6:c.607C>G ENSP00000427089.2:p.Gln203Glu
ENST00000508624.5:c.607C>G ENSP00000424265.1:p.Gln203Glu
ENST00000512211.6:c.607C>G ENSP00000423828.2:p.Gln203Glu
NM_000038.5:c.607C>G NP_000029.2:p.Gln203Glu
NM_001127510.2:c.607C>G NP_001120982.1:p.Gln203Glu
NM_001127511.2:c.637C>G NP_001120983.2:p.Gln213Glu
NM_001354895.1:c.607C>G NP_001341824.1:p.Gln203Glu
NM_001354896.1:c.607C>G NP_001341825.1:p.Gln203Glu
NM_001354897.1:c.637C>G NP_001341826.1:p.Gln213Glu
NM_001354898.1:c.532C>G NP_001341827.1:p.Gln178Glu
NM_001354899.1:c.607C>G NP_001341828.1:p.Gln203Glu
NM_001354900.1:c.430C>G NP_001341829.1:p.Gln144Glu
NM_001354901.1:c.430C>G NP_001341830.1:p.Gln144Glu
NM_001354902.1:c.637C>G NP_001341831.1:p.Gln213Glu
NM_001354903.1:c.607C>G NP_001341832.1:p.Gln203Glu
NM_001354904.1:c.532C>G NP_001341833.1:p.Gln178Glu
NM_001354905.1:c.430C>G NP_001341834.1:p.Gln144Glu
NM_001354906.1:c.-429C>G NP_001341835.1:n.-429C>G
NM_000038.6:c.607C>G MANE Select NP_000029.2:p.Gln203Glu
NM_001127510.3:c.607C>G NP_001120982.1:p.Gln203Glu
NM_001127511.3:c.637C>G NP_001120983.2:p.Gln213Glu
NM_001354895.2:c.607C>G NP_001341824.1:p.Gln203Glu
NM_001354896.2:c.607C>G NP_001341825.1:p.Gln203Glu
NM_001354897.2:c.637C>G NP_001341826.1:p.Gln213Glu
NM_001354898.2:c.532C>G NP_001341827.1:p.Gln178Glu
NM_001354899.2:c.607C>G NP_001341828.1:p.Gln203Glu
NM_001354900.2:c.430C>G NP_001341829.1:p.Gln144Glu
NM_001354901.2:c.430C>G NP_001341830.1:p.Gln144Glu
NM_001354902.2:c.637C>G NP_001341831.1:p.Gln213Glu
NM_001354903.2:c.607C>G NP_001341832.1:p.Gln203Glu
NM_001354904.2:c.532C>G NP_001341833.1:p.Gln178Glu
NM_001354905.2:c.430C>G NP_001341834.1:p.Gln144Glu
NM_001354906.2:c.-429C>G NP_001341835.1:n.-429C>G