Canonical Allele Identifier: CA16032373

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112176340A>T (hg19) ; chr5:g.112840643A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840643A>T , CM000667.2:g.112840643A>T	GRCh38
NC_000005.9:g.112176340A>T , CM000667.1:g.112176340A>T	GRCh37
NC_000005.8:g.112204239A>T	NCBI36
NG_008481.4:g.153123A>T , LRG_130:g.153123A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5103A>T	ENSP00000473355.2:p.Glu1701Asp
ENST00000505350.2:c.*5055A>T	ENSP00000481752.1:n.*5055A>T
ENST00000507379.6:c.4995A>T	ENSP00000423224.2:p.Glu1665Asp
ENST00000509732.6:c.5049A>T	ENSP00000426541.2:p.Glu1683Asp
ENST00000512211.7:c.5049A>T	ENSP00000423828.3:p.Glu1683Asp
ENST00000257430.9:c.5049A>T MANE Select	ENSP00000257430.4:p.Glu1683Asp
ENST00000257430.8:c.5049A>T	ENSP00000257430.4:p.Glu1683Asp
ENST00000508376.6:c.5049A>T	ENSP00000427089.2:p.Glu1683Asp
ENST00000508624.5:c.*4371A>T	ENSP00000424265.1:n.*4371A>T
ENST00000520401.1:c.230+11671A>T
NM_000038.5:c.5049A>T	NP_000029.2:p.Glu1683Asp
NM_001127510.2:c.5049A>T	NP_001120982.1:p.Glu1683Asp
NM_001127511.2:c.4995A>T	NP_001120983.2:p.Glu1665Asp
NM_001354895.1:c.5049A>T	NP_001341824.1:p.Glu1683Asp
NM_001354896.1:c.5103A>T	NP_001341825.1:p.Glu1701Asp
NM_001354897.1:c.5079A>T	NP_001341826.1:p.Glu1693Asp
NM_001354898.1:c.4974A>T	NP_001341827.1:p.Glu1658Asp
NM_001354899.1:c.4965A>T	NP_001341828.1:p.Glu1655Asp
NM_001354900.1:c.4926A>T	NP_001341829.1:p.Glu1642Asp
NM_001354901.1:c.4872A>T	NP_001341830.1:p.Glu1624Asp
NM_001354902.1:c.4776A>T	NP_001341831.1:p.Glu1592Asp
NM_001354903.1:c.4746A>T	NP_001341832.1:p.Glu1582Asp
NM_001354904.1:c.4671A>T	NP_001341833.1:p.Glu1557Asp
NM_001354905.1:c.4569A>T	NP_001341834.1:p.Glu1523Asp
NM_001354906.1:c.4200A>T	NP_001341835.1:p.Glu1400Asp
NM_000038.6:c.5049A>T MANE Select	NP_000029.2:p.Glu1683Asp
NM_001127510.3:c.5049A>T	NP_001120982.1:p.Glu1683Asp
NM_001127511.3:c.4995A>T	NP_001120983.2:p.Glu1665Asp
NM_001354895.2:c.5049A>T	NP_001341824.1:p.Glu1683Asp
NM_001354896.2:c.5103A>T	NP_001341825.1:p.Glu1701Asp
NM_001354897.2:c.5079A>T	NP_001341826.1:p.Glu1693Asp
NM_001354898.2:c.4974A>T	NP_001341827.1:p.Glu1658Asp
NM_001354899.2:c.4965A>T	NP_001341828.1:p.Glu1655Asp
NM_001354900.2:c.4926A>T	NP_001341829.1:p.Glu1642Asp
NM_001354901.2:c.4872A>T	NP_001341830.1:p.Glu1624Asp
NM_001354902.2:c.4776A>T	NP_001341831.1:p.Glu1592Asp
NM_001354903.2:c.4746A>T	NP_001341832.1:p.Glu1582Asp
NM_001354904.2:c.4671A>T	NP_001341833.1:p.Glu1557Asp
NM_001354905.2:c.4569A>T	NP_001341834.1:p.Glu1523Asp
NM_001354906.2:c.4200A>T	NP_001341835.1:p.Glu1400Asp