Canonical Allele Identifier: CA16024514

Gene: APC

Linked Data

• dbSNP Id: rs2149809299
• MyVariant Identifiers: chr5:g.112162862C>G (hg19) ; chr5:g.112827165C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112827165C>G , CM000667.2:g.112827165C>G	GRCh38
NC_000005.9:g.112162862C>G , CM000667.1:g.112162862C>G	GRCh37
NC_000005.8:g.112190761C>G	NCBI36
NG_008481.4:g.139645C>G , LRG_130:g.139645C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1408+5174C>G	ENSP00000484935.2:n.1408+5174C>G
ENST00000504915.3:c.1520C>G	ENSP00000473355.2:p.Thr507Ser
ENST00000505084.2:n.1522C>G
ENST00000505350.2:c.*1472C>G	ENSP00000481752.1:n.*1472C>G
ENST00000507379.6:c.1412C>G	ENSP00000423224.2:p.Thr471Ser
ENST00000509732.6:c.1466C>G	ENSP00000426541.2:p.Thr489Ser
ENST00000512211.7:c.1466C>G	ENSP00000423828.3:p.Thr489Ser
ENST00000257430.9:c.1466C>G MANE Select	ENSP00000257430.4:p.Thr489Ser
ENST00000257430.8:c.1466C>G	ENSP00000257430.4:p.Thr489Ser
ENST00000502371.2:c.96+5174C>G
ENST00000504915.2:c.155C>G	ENSP00000473355.1:p.Thr52Ser
ENST00000507379.5:c.1412C>G	ENSP00000423224.1:p.Thr471Ser
ENST00000508376.6:c.1466C>G	ENSP00000427089.2:p.Thr489Ser
ENST00000508624.5:c.*788C>G	ENSP00000424265.1:n.*788C>G
ENST00000512211.6:c.1466C>G	ENSP00000423828.2:p.Thr489Ser
NM_000038.5:c.1466C>G	NP_000029.2:p.Thr489Ser
NM_001127510.2:c.1466C>G	NP_001120982.1:p.Thr489Ser
NM_001127511.2:c.1412C>G	NP_001120983.2:p.Thr471Ser
NM_001354895.1:c.1466C>G	NP_001341824.1:p.Thr489Ser
NM_001354896.1:c.1520C>G	NP_001341825.1:p.Thr507Ser
NM_001354897.1:c.1496C>G	NP_001341826.1:p.Thr499Ser
NM_001354898.1:c.1391C>G	NP_001341827.1:p.Thr464Ser
NM_001354899.1:c.1382C>G	NP_001341828.1:p.Thr461Ser
NM_001354900.1:c.1343C>G	NP_001341829.1:p.Thr448Ser
NM_001354901.1:c.1289C>G	NP_001341830.1:p.Thr430Ser
NM_001354902.1:c.1193C>G	NP_001341831.1:p.Thr398Ser
NM_001354903.1:c.1163C>G	NP_001341832.1:p.Thr388Ser
NM_001354904.1:c.1088C>G	NP_001341833.1:p.Thr363Ser
NM_001354905.1:c.986C>G	NP_001341834.1:p.Thr329Ser
NM_001354906.1:c.617C>G	NP_001341835.1:p.Thr206Ser
NM_000038.6:c.1466C>G MANE Select	NP_000029.2:p.Thr489Ser
NM_001127510.3:c.1466C>G	NP_001120982.1:p.Thr489Ser
NM_001127511.3:c.1412C>G	NP_001120983.2:p.Thr471Ser
NM_001354895.2:c.1466C>G	NP_001341824.1:p.Thr489Ser
NM_001354896.2:c.1520C>G	NP_001341825.1:p.Thr507Ser
NM_001354897.2:c.1496C>G	NP_001341826.1:p.Thr499Ser
NM_001354898.2:c.1391C>G	NP_001341827.1:p.Thr464Ser
NM_001354899.2:c.1382C>G	NP_001341828.1:p.Thr461Ser
NM_001354900.2:c.1343C>G	NP_001341829.1:p.Thr448Ser
NM_001354901.2:c.1289C>G	NP_001341830.1:p.Thr430Ser
NM_001354902.2:c.1193C>G	NP_001341831.1:p.Thr398Ser
NM_001354903.2:c.1163C>G	NP_001341832.1:p.Thr388Ser
NM_001354904.2:c.1088C>G	NP_001341833.1:p.Thr363Ser
NM_001354905.2:c.986C>G	NP_001341834.1:p.Thr329Ser
NM_001354906.2:c.617C>G	NP_001341835.1:p.Thr206Ser