Canonical Allele Identifier: CA446209682

Gene: APC

Linked Data

• dbSNP Id: rs1554086592
• MyVariant Identifiers: chr5:g.112176571C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840874C>T , CM000667.2:g.112840874C>T	GRCh38
NC_000005.9:g.112176571C>T , CM000667.1:g.112176571C>T	GRCh37
NC_000005.8:g.112204470C>T	NCBI36
NG_008481.4:g.153354C>T , LRG_130:g.153354C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5334C>T	ENSP00000473355.2:p.Pro1778=
ENST00000505350.2:c.*5286C>T	ENSP00000481752.1:n.*5286C>T
ENST00000507379.6:c.5226C>T	ENSP00000423224.2:p.Pro1742=
ENST00000509732.6:c.5280C>T	ENSP00000426541.2:p.Pro1760=
ENST00000512211.7:c.5280C>T	ENSP00000423828.3:p.Pro1760=
ENST00000257430.9:c.5280C>T MANE Select	ENSP00000257430.4:p.Pro1760=
ENST00000257430.8:c.5280C>T	ENSP00000257430.4:p.Pro1760=
ENST00000508376.6:c.5280C>T	ENSP00000427089.2:p.Pro1760=
ENST00000508624.5:c.*4602C>T	ENSP00000424265.1:n.*4602C>T
ENST00000520401.1:c.230+11902C>T
NM_000038.5:c.5280C>T	NP_000029.2:p.Pro1760=
NM_001127510.2:c.5280C>T	NP_001120982.1:p.Pro1760=
NM_001127511.2:c.5226C>T	NP_001120983.2:p.Pro1742=
NM_001354895.1:c.5280C>T	NP_001341824.1:p.Pro1760=
NM_001354896.1:c.5334C>T	NP_001341825.1:p.Pro1778=
NM_001354897.1:c.5310C>T	NP_001341826.1:p.Pro1770=
NM_001354898.1:c.5205C>T	NP_001341827.1:p.Pro1735=
NM_001354899.1:c.5196C>T	NP_001341828.1:p.Pro1732=
NM_001354900.1:c.5157C>T	NP_001341829.1:p.Pro1719=
NM_001354901.1:c.5103C>T	NP_001341830.1:p.Pro1701=
NM_001354902.1:c.5007C>T	NP_001341831.1:p.Pro1669=
NM_001354903.1:c.4977C>T	NP_001341832.1:p.Pro1659=
NM_001354904.1:c.4902C>T	NP_001341833.1:p.Pro1634=
NM_001354905.1:c.4800C>T	NP_001341834.1:p.Pro1600=
NM_001354906.1:c.4431C>T	NP_001341835.1:p.Pro1477=
NM_000038.6:c.5280C>T MANE Select	NP_000029.2:p.Pro1760=
NM_001127510.3:c.5280C>T	NP_001120982.1:p.Pro1760=
NM_001127511.3:c.5226C>T	NP_001120983.2:p.Pro1742=
NM_001354895.2:c.5280C>T	NP_001341824.1:p.Pro1760=
NM_001354896.2:c.5334C>T	NP_001341825.1:p.Pro1778=
NM_001354897.2:c.5310C>T	NP_001341826.1:p.Pro1770=
NM_001354898.2:c.5205C>T	NP_001341827.1:p.Pro1735=
NM_001354899.2:c.5196C>T	NP_001341828.1:p.Pro1732=
NM_001354900.2:c.5157C>T	NP_001341829.1:p.Pro1719=
NM_001354901.2:c.5103C>T	NP_001341830.1:p.Pro1701=
NM_001354902.2:c.5007C>T	NP_001341831.1:p.Pro1669=
NM_001354903.2:c.4977C>T	NP_001341832.1:p.Pro1659=
NM_001354904.2:c.4902C>T	NP_001341833.1:p.Pro1634=
NM_001354905.2:c.4800C>T	NP_001341834.1:p.Pro1600=
NM_001354906.2:c.4431C>T	NP_001341835.1:p.Pro1477=