Canonical Allele Identifier: CA16034365
Community Standard Title: NM_000038.6(APC):c.5953G>T (p.Glu1985Ter)
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112841547G>T , CM000667.2:g.112841547G>T GRCh38
NC_000005.9:g.112177244G>T , CM000667.1:g.112177244G>T GRCh37
NC_000005.8:g.112205143G>T NCBI36
NG_008481.4:g.154027G>T , LRG_130:g.154027G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000038.6:c.5953G>T MANE Select NP_000029.2:p.Glu1985Ter
ENST00000257430.9:c.5953G>T MANE Select ENSP00000257430.4:p.Glu1985Ter
NM_000038.5:c.5953G>T NP_000029.2:p.Glu1985Ter
NM_001127510.2:c.5953G>T NP_001120982.1:p.Glu1985Ter
NM_001127510.3:c.5953G>T NP_001120982.1:p.Glu1985Ter
NM_001127511.2:c.5899G>T NP_001120983.2:p.Glu1967Ter
NM_001127511.3:c.5899G>T NP_001120983.2:p.Glu1967Ter
NM_001354895.1:c.5953G>T NP_001341824.1:p.Glu1985Ter
NM_001354895.2:c.5953G>T NP_001341824.1:p.Glu1985Ter
NM_001354896.1:c.6007G>T NP_001341825.1:p.Glu2003Ter
NM_001354896.2:c.6007G>T NP_001341825.1:p.Glu2003Ter
NM_001354897.1:c.5983G>T NP_001341826.1:p.Glu1995Ter
NM_001354897.2:c.5983G>T NP_001341826.1:p.Glu1995Ter
NM_001354898.1:c.5878G>T NP_001341827.1:p.Glu1960Ter
NM_001354898.2:c.5878G>T NP_001341827.1:p.Glu1960Ter
NM_001354899.1:c.5869G>T NP_001341828.1:p.Glu1957Ter
NM_001354899.2:c.5869G>T NP_001341828.1:p.Glu1957Ter
NM_001354900.1:c.5830G>T NP_001341829.1:p.Glu1944Ter
NM_001354900.2:c.5830G>T NP_001341829.1:p.Glu1944Ter
NM_001354901.1:c.5776G>T NP_001341830.1:p.Glu1926Ter
NM_001354901.2:c.5776G>T NP_001341830.1:p.Glu1926Ter
NM_001354902.1:c.5680G>T NP_001341831.1:p.Glu1894Ter
NM_001354902.2:c.5680G>T NP_001341831.1:p.Glu1894Ter
NM_001354903.1:c.5650G>T NP_001341832.1:p.Glu1884Ter
NM_001354903.2:c.5650G>T NP_001341832.1:p.Glu1884Ter
NM_001354904.1:c.5575G>T NP_001341833.1:p.Glu1859Ter
NM_001354904.2:c.5575G>T NP_001341833.1:p.Glu1859Ter
NM_001354905.1:c.5473G>T NP_001341834.1:p.Glu1825Ter
NM_001354905.2:c.5473G>T NP_001341834.1:p.Glu1825Ter
NM_001354906.1:c.5104G>T NP_001341835.1:p.Glu1702Ter
NM_001354906.2:c.5104G>T NP_001341835.1:p.Glu1702Ter
ENST00000257430.8:c.5953G>T ENSP00000257430.4:p.Glu1985Ter
ENST00000504915.3:c.6007G>T ENSP00000473355.2:p.Glu2003Ter
ENST00000505350.2:c.*5959G>T ENSP00000481752.1:n.*5959G>T
ENST00000507379.6:c.5899G>T ENSP00000423224.2:p.Glu1967Ter
ENST00000508376.6:c.5953G>T ENSP00000427089.2:p.Glu1985Ter
ENST00000508624.5:c.*5275G>T ENSP00000424265.1:n.*5275G>T
ENST00000509732.6:c.5953G>T ENSP00000426541.2:p.Glu1985Ter
ENST00000512211.7:c.5953G>T ENSP00000423828.3:p.Glu1985Ter
ENST00000520401.1:c.230+12575G>T