Canonical Allele Identifier: CA16023840
Gene: APC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112819189C>T , CM000667.2:g.112819189C>T GRCh38
NC_000005.9:g.112154886C>T , CM000667.1:g.112154886C>T GRCh37
NC_000005.8:g.112182785C>T NCBI36
NG_008481.4:g.131669C>T , LRG_130:g.131669C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000502371.3:c.1157C>T ENSP00000484935.2:p.Ala386Val
ENST00000504915.3:c.1157C>T ENSP00000473355.2:p.Ala386Val
ENST00000505084.2:n.1213C>T
ENST00000505350.2:c.*1163C>T ENSP00000481752.1:n.*1163C>T
ENST00000507379.6:c.1103C>T ENSP00000423224.2:p.Ala368Val
ENST00000509732.6:c.1157C>T ENSP00000426541.2:p.Ala386Val
ENST00000512211.7:c.1157C>T ENSP00000423828.3:p.Ala386Val
ENST00000257430.9:c.1157C>T MANE Select ENSP00000257430.4:p.Ala386Val
ENST00000257430.8:c.1157C>T ENSP00000257430.4:p.Ala386Val
ENST00000507379.5:c.1103C>T ENSP00000423224.1:p.Ala368Val
ENST00000508376.6:c.1157C>T ENSP00000427089.2:p.Ala386Val
ENST00000508624.5:c.*479C>T ENSP00000424265.1:n.*479C>T
ENST00000512211.6:c.1157C>T ENSP00000423828.2:p.Ala386Val
NM_000038.5:c.1157C>T NP_000029.2:p.Ala386Val
NM_001127510.2:c.1157C>T NP_001120982.1:p.Ala386Val
NM_001127511.2:c.1103C>T NP_001120983.2:p.Ala368Val
NM_001354895.1:c.1157C>T NP_001341824.1:p.Ala386Val
NM_001354896.1:c.1157C>T NP_001341825.1:p.Ala386Val
NM_001354897.1:c.1187C>T NP_001341826.1:p.Ala396Val
NM_001354898.1:c.1082C>T NP_001341827.1:p.Ala361Val
NM_001354899.1:c.1073C>T NP_001341828.1:p.Ala358Val
NM_001354900.1:c.980C>T NP_001341829.1:p.Ala327Val
NM_001354901.1:c.980C>T NP_001341830.1:p.Ala327Val
NM_001354902.1:c.964-80C>T NP_001341831.1:n.964-80C>T
NM_001354903.1:c.934-80C>T NP_001341832.1:n.934-80C>T
NM_001354904.1:c.859-80C>T NP_001341833.1:n.859-80C>T
NM_001354905.1:c.757-80C>T NP_001341834.1:n.757-80C>T
NM_001354906.1:c.308C>T NP_001341835.1:p.Ala103Val
NM_000038.6:c.1157C>T MANE Select NP_000029.2:p.Ala386Val
NM_001127510.3:c.1157C>T NP_001120982.1:p.Ala386Val
NM_001127511.3:c.1103C>T NP_001120983.2:p.Ala368Val
NM_001354895.2:c.1157C>T NP_001341824.1:p.Ala386Val
NM_001354896.2:c.1157C>T NP_001341825.1:p.Ala386Val
NM_001354897.2:c.1187C>T NP_001341826.1:p.Ala396Val
NM_001354898.2:c.1082C>T NP_001341827.1:p.Ala361Val
NM_001354899.2:c.1073C>T NP_001341828.1:p.Ala358Val
NM_001354900.2:c.980C>T NP_001341829.1:p.Ala327Val
NM_001354901.2:c.980C>T NP_001341830.1:p.Ala327Val
NM_001354902.2:c.964-80C>T NP_001341831.1:n.964-80C>T
NM_001354903.2:c.934-80C>T NP_001341832.1:n.934-80C>T
NM_001354904.2:c.859-80C>T NP_001341833.1:n.859-80C>T
NM_001354905.2:c.757-80C>T NP_001341834.1:n.757-80C>T
NM_001354906.2:c.308C>T NP_001341835.1:p.Ala103Val