Canonical Allele Identifier: CA16026407

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112173606C>A (hg19) ; chr5:g.112837909C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112837909C>A , CM000667.2:g.112837909C>A	GRCh38
NC_000005.9:g.112173606C>A , CM000667.1:g.112173606C>A	GRCh37
NC_000005.8:g.112201505C>A	NCBI36
NG_008481.4:g.150389C>A , LRG_130:g.150389C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1980C>A	ENSP00000484935.2:n.1980C>A
ENST00000504915.3:c.2369C>A	ENSP00000473355.2:p.Thr790Asn
ENST00000505350.2:c.*2321C>A	ENSP00000481752.1:n.*2321C>A
ENST00000507379.6:c.2261C>A	ENSP00000423224.2:p.Thr754Asn
ENST00000509732.6:c.2315C>A	ENSP00000426541.2:p.Thr772Asn
ENST00000512211.7:c.2315C>A	ENSP00000423828.3:p.Thr772Asn
ENST00000257430.9:c.2315C>A MANE Select	ENSP00000257430.4:p.Thr772Asn
ENST00000257430.8:c.2315C>A	ENSP00000257430.4:p.Thr772Asn
ENST00000502371.2:c.668C>A
ENST00000507379.5:c.2261C>A	ENSP00000423224.1:p.Thr754Asn
ENST00000508376.6:c.2315C>A	ENSP00000427089.2:p.Thr772Asn
ENST00000508624.5:c.*1637C>A	ENSP00000424265.1:n.*1637C>A
ENST00000512211.6:c.2315C>A	ENSP00000423828.2:p.Thr772Asn
ENST00000520401.1:c.230+8937C>A
NM_000038.5:c.2315C>A	NP_000029.2:p.Thr772Asn
NM_001127510.2:c.2315C>A	NP_001120982.1:p.Thr772Asn
NM_001127511.2:c.2261C>A	NP_001120983.2:p.Thr754Asn
NM_001354895.1:c.2315C>A	NP_001341824.1:p.Thr772Asn
NM_001354896.1:c.2369C>A	NP_001341825.1:p.Thr790Asn
NM_001354897.1:c.2345C>A	NP_001341826.1:p.Thr782Asn
NM_001354898.1:c.2240C>A	NP_001341827.1:p.Thr747Asn
NM_001354899.1:c.2231C>A	NP_001341828.1:p.Thr744Asn
NM_001354900.1:c.2192C>A	NP_001341829.1:p.Thr731Asn
NM_001354901.1:c.2138C>A	NP_001341830.1:p.Thr713Asn
NM_001354902.1:c.2042C>A	NP_001341831.1:p.Thr681Asn
NM_001354903.1:c.2012C>A	NP_001341832.1:p.Thr671Asn
NM_001354904.1:c.1937C>A	NP_001341833.1:p.Thr646Asn
NM_001354905.1:c.1835C>A	NP_001341834.1:p.Thr612Asn
NM_001354906.1:c.1466C>A	NP_001341835.1:p.Thr489Asn
NM_000038.6:c.2315C>A MANE Select	NP_000029.2:p.Thr772Asn
NM_001127510.3:c.2315C>A	NP_001120982.1:p.Thr772Asn
NM_001127511.3:c.2261C>A	NP_001120983.2:p.Thr754Asn
NM_001354895.2:c.2315C>A	NP_001341824.1:p.Thr772Asn
NM_001354896.2:c.2369C>A	NP_001341825.1:p.Thr790Asn
NM_001354897.2:c.2345C>A	NP_001341826.1:p.Thr782Asn
NM_001354898.2:c.2240C>A	NP_001341827.1:p.Thr747Asn
NM_001354899.2:c.2231C>A	NP_001341828.1:p.Thr744Asn
NM_001354900.2:c.2192C>A	NP_001341829.1:p.Thr731Asn
NM_001354901.2:c.2138C>A	NP_001341830.1:p.Thr713Asn
NM_001354902.2:c.2042C>A	NP_001341831.1:p.Thr681Asn
NM_001354903.2:c.2012C>A	NP_001341832.1:p.Thr671Asn
NM_001354904.2:c.1937C>A	NP_001341833.1:p.Thr646Asn
NM_001354905.2:c.1835C>A	NP_001341834.1:p.Thr612Asn
NM_001354906.2:c.1466C>A	NP_001341835.1:p.Thr489Asn