Canonical Allele Identifier: CA16031440

Gene: APC

Linked Data

• dbSNP Id: rs786201181
• MyVariant Identifiers: chr5:g.112175905A>T (hg19) ; chr5:g.112840208A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840208A>T , CM000667.2:g.112840208A>T	GRCh38
NC_000005.9:g.112175905A>T , CM000667.1:g.112175905A>T	GRCh37
NC_000005.8:g.112203804A>T	NCBI36
NG_008481.4:g.152688A>T , LRG_130:g.152688A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4668A>T	ENSP00000473355.2:p.Glu1556Asp
ENST00000505350.2:c.*4620A>T	ENSP00000481752.1:n.*4620A>T
ENST00000507379.6:c.4560A>T	ENSP00000423224.2:p.Glu1520Asp
ENST00000509732.6:c.4614A>T	ENSP00000426541.2:p.Glu1538Asp
ENST00000512211.7:c.4614A>T	ENSP00000423828.3:p.Glu1538Asp
ENST00000257430.9:c.4614A>T MANE Select	ENSP00000257430.4:p.Glu1538Asp
ENST00000257430.8:c.4614A>T	ENSP00000257430.4:p.Glu1538Asp
ENST00000508376.6:c.4614A>T	ENSP00000427089.2:p.Glu1538Asp
ENST00000508624.5:c.*3936A>T	ENSP00000424265.1:n.*3936A>T
ENST00000520401.1:c.230+11236A>T
NM_000038.5:c.4614A>T	NP_000029.2:p.Glu1538Asp
NM_001127510.2:c.4614A>T	NP_001120982.1:p.Glu1538Asp
NM_001127511.2:c.4560A>T	NP_001120983.2:p.Glu1520Asp
NM_001354895.1:c.4614A>T	NP_001341824.1:p.Glu1538Asp
NM_001354896.1:c.4668A>T	NP_001341825.1:p.Glu1556Asp
NM_001354897.1:c.4644A>T	NP_001341826.1:p.Glu1548Asp
NM_001354898.1:c.4539A>T	NP_001341827.1:p.Glu1513Asp
NM_001354899.1:c.4530A>T	NP_001341828.1:p.Glu1510Asp
NM_001354900.1:c.4491A>T	NP_001341829.1:p.Glu1497Asp
NM_001354901.1:c.4437A>T	NP_001341830.1:p.Glu1479Asp
NM_001354902.1:c.4341A>T	NP_001341831.1:p.Glu1447Asp
NM_001354903.1:c.4311A>T	NP_001341832.1:p.Glu1437Asp
NM_001354904.1:c.4236A>T	NP_001341833.1:p.Glu1412Asp
NM_001354905.1:c.4134A>T	NP_001341834.1:p.Glu1378Asp
NM_001354906.1:c.3765A>T	NP_001341835.1:p.Glu1255Asp
NM_000038.6:c.4614A>T MANE Select	NP_000029.2:p.Glu1538Asp
NM_001127510.3:c.4614A>T	NP_001120982.1:p.Glu1538Asp
NM_001127511.3:c.4560A>T	NP_001120983.2:p.Glu1520Asp
NM_001354895.2:c.4614A>T	NP_001341824.1:p.Glu1538Asp
NM_001354896.2:c.4668A>T	NP_001341825.1:p.Glu1556Asp
NM_001354897.2:c.4644A>T	NP_001341826.1:p.Glu1548Asp
NM_001354898.2:c.4539A>T	NP_001341827.1:p.Glu1513Asp
NM_001354899.2:c.4530A>T	NP_001341828.1:p.Glu1510Asp
NM_001354900.2:c.4491A>T	NP_001341829.1:p.Glu1497Asp
NM_001354901.2:c.4437A>T	NP_001341830.1:p.Glu1479Asp
NM_001354902.2:c.4341A>T	NP_001341831.1:p.Glu1447Asp
NM_001354903.2:c.4311A>T	NP_001341832.1:p.Glu1437Asp
NM_001354904.2:c.4236A>T	NP_001341833.1:p.Glu1412Asp
NM_001354905.2:c.4134A>T	NP_001341834.1:p.Glu1378Asp
NM_001354906.2:c.3765A>T	NP_001341835.1:p.Glu1255Asp