Canonical Allele Identifier: CA16024434

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112827128G>T , CM000667.2:g.112827128G>T	GRCh38
NC_000005.9:g.112162825G>T , CM000667.1:g.112162825G>T	GRCh37
NC_000005.8:g.112190724G>T	NCBI36
NG_008481.4:g.139608G>T , LRG_130:g.139608G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000038.6:c.1429G>T MANE Select	NP_000029.2:p.Glu477Ter
ENST00000257430.9:c.1429G>T MANE Select	ENSP00000257430.4:p.Glu477Ter
NM_000038.5:c.1429G>T	NP_000029.2:p.Glu477Ter
NM_001127510.2:c.1429G>T	NP_001120982.1:p.Glu477Ter
NM_001127510.3:c.1429G>T	NP_001120982.1:p.Glu477Ter
NM_001127511.2:c.1375G>T	NP_001120983.2:p.Glu459Ter
NM_001127511.3:c.1375G>T	NP_001120983.2:p.Glu459Ter
NM_001354895.1:c.1429G>T	NP_001341824.1:p.Glu477Ter
NM_001354895.2:c.1429G>T	NP_001341824.1:p.Glu477Ter
NM_001354896.1:c.1483G>T	NP_001341825.1:p.Glu495Ter
NM_001354896.2:c.1483G>T	NP_001341825.1:p.Glu495Ter
NM_001354897.1:c.1459G>T	NP_001341826.1:p.Glu487Ter
NM_001354897.2:c.1459G>T	NP_001341826.1:p.Glu487Ter
NM_001354898.1:c.1354G>T	NP_001341827.1:p.Glu452Ter
NM_001354898.2:c.1354G>T	NP_001341827.1:p.Glu452Ter
NM_001354899.1:c.1345G>T	NP_001341828.1:p.Glu449Ter
NM_001354899.2:c.1345G>T	NP_001341828.1:p.Glu449Ter
NM_001354900.1:c.1306G>T	NP_001341829.1:p.Glu436Ter
NM_001354900.2:c.1306G>T	NP_001341829.1:p.Glu436Ter
NM_001354901.1:c.1252G>T	NP_001341830.1:p.Glu418Ter
NM_001354901.2:c.1252G>T	NP_001341830.1:p.Glu418Ter
NM_001354902.1:c.1156G>T	NP_001341831.1:p.Glu386Ter
NM_001354902.2:c.1156G>T	NP_001341831.1:p.Glu386Ter
NM_001354903.1:c.1126G>T	NP_001341832.1:p.Glu376Ter
NM_001354903.2:c.1126G>T	NP_001341832.1:p.Glu376Ter
NM_001354904.1:c.1051G>T	NP_001341833.1:p.Glu351Ter
NM_001354904.2:c.1051G>T	NP_001341833.1:p.Glu351Ter
NM_001354905.1:c.949G>T	NP_001341834.1:p.Glu317Ter
NM_001354905.2:c.949G>T	NP_001341834.1:p.Glu317Ter
NM_001354906.1:c.580G>T	NP_001341835.1:p.Glu194Ter
NM_001354906.2:c.580G>T	NP_001341835.1:p.Glu194Ter
ENST00000257430.8:c.1429G>T	ENSP00000257430.4:p.Glu477Ter
ENST00000502371.2:c.96+5137G>T
ENST00000502371.3:c.1408+5137G>T	ENSP00000484935.2:n.1408+5137G>T
ENST00000504915.2:c.118G>T	ENSP00000473355.1:p.Glu40Ter
ENST00000504915.3:c.1483G>T	ENSP00000473355.2:p.Glu495Ter
ENST00000505084.2:n.1485G>T
ENST00000505350.2:c.*1435G>T	ENSP00000481752.1:n.*1435G>T
ENST00000507379.5:c.1375G>T	ENSP00000423224.1:p.Glu459Ter
ENST00000507379.6:c.1375G>T	ENSP00000423224.2:p.Glu459Ter
ENST00000508376.6:c.1429G>T	ENSP00000427089.2:p.Glu477Ter
ENST00000508624.5:c.*751G>T	ENSP00000424265.1:n.*751G>T
ENST00000509732.6:c.1429G>T	ENSP00000426541.2:p.Glu477Ter
ENST00000512211.6:c.1429G>T	ENSP00000423828.2:p.Glu477Ter
ENST00000512211.7:c.1429G>T	ENSP00000423828.3:p.Glu477Ter