Canonical Allele Identifier: CA16025579

Gene: APC

Linked Data

• dbSNP Id: rs1416247275
• MyVariant Identifiers: chr5:g.112170854G>T (hg19) ; chr5:g.112835157G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112835157G>T , CM000667.2:g.112835157G>T	GRCh38
NC_000005.9:g.112170854G>T , CM000667.1:g.112170854G>T	GRCh37
NC_000005.8:g.112198753G>T	NCBI36
NG_008481.4:g.147637G>T , LRG_130:g.147637G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1615G>T	ENSP00000484935.2:n.1615G>T
ENST00000504915.3:c.2004G>T	ENSP00000473355.2:p.Glu668Asp
ENST00000505350.2:c.*1956G>T	ENSP00000481752.1:n.*1956G>T
ENST00000507379.6:c.1896G>T	ENSP00000423224.2:p.Glu632Asp
ENST00000509732.6:c.1950G>T	ENSP00000426541.2:p.Glu650Asp
ENST00000512211.7:c.1950G>T	ENSP00000423828.3:p.Glu650Asp
ENST00000257430.9:c.1950G>T MANE Select	ENSP00000257430.4:p.Glu650Asp
ENST00000257430.8:c.1950G>T	ENSP00000257430.4:p.Glu650Asp
ENST00000502371.2:c.303G>T
ENST00000504915.2:c.639G>T	ENSP00000473355.1:p.Glu213Asp
ENST00000507379.5:c.1896G>T	ENSP00000423224.1:p.Glu632Asp
ENST00000508376.6:c.1950G>T	ENSP00000427089.2:p.Glu650Asp
ENST00000508624.5:c.*1272G>T	ENSP00000424265.1:n.*1272G>T
ENST00000512211.6:c.1950G>T	ENSP00000423828.2:p.Glu650Asp
ENST00000520401.1:c.230+6185G>T
NM_000038.5:c.1950G>T	NP_000029.2:p.Glu650Asp
NM_001127510.2:c.1950G>T	NP_001120982.1:p.Glu650Asp
NM_001127511.2:c.1896G>T	NP_001120983.2:p.Glu632Asp
NM_001354895.1:c.1950G>T	NP_001341824.1:p.Glu650Asp
NM_001354896.1:c.2004G>T	NP_001341825.1:p.Glu668Asp
NM_001354897.1:c.1980G>T	NP_001341826.1:p.Glu660Asp
NM_001354898.1:c.1875G>T	NP_001341827.1:p.Glu625Asp
NM_001354899.1:c.1866G>T	NP_001341828.1:p.Glu622Asp
NM_001354900.1:c.1827G>T	NP_001341829.1:p.Glu609Asp
NM_001354901.1:c.1773G>T	NP_001341830.1:p.Glu591Asp
NM_001354902.1:c.1677G>T	NP_001341831.1:p.Glu559Asp
NM_001354903.1:c.1647G>T	NP_001341832.1:p.Glu549Asp
NM_001354904.1:c.1572G>T	NP_001341833.1:p.Glu524Asp
NM_001354905.1:c.1470G>T	NP_001341834.1:p.Glu490Asp
NM_001354906.1:c.1101G>T	NP_001341835.1:p.Glu367Asp
NM_000038.6:c.1950G>T MANE Select	NP_000029.2:p.Glu650Asp
NM_001127510.3:c.1950G>T	NP_001120982.1:p.Glu650Asp
NM_001127511.3:c.1896G>T	NP_001120983.2:p.Glu632Asp
NM_001354895.2:c.1950G>T	NP_001341824.1:p.Glu650Asp
NM_001354896.2:c.2004G>T	NP_001341825.1:p.Glu668Asp
NM_001354897.2:c.1980G>T	NP_001341826.1:p.Glu660Asp
NM_001354898.2:c.1875G>T	NP_001341827.1:p.Glu625Asp
NM_001354899.2:c.1866G>T	NP_001341828.1:p.Glu622Asp
NM_001354900.2:c.1827G>T	NP_001341829.1:p.Glu609Asp
NM_001354901.2:c.1773G>T	NP_001341830.1:p.Glu591Asp
NM_001354902.2:c.1677G>T	NP_001341831.1:p.Glu559Asp
NM_001354903.2:c.1647G>T	NP_001341832.1:p.Glu549Asp
NM_001354904.2:c.1572G>T	NP_001341833.1:p.Glu524Asp
NM_001354905.2:c.1470G>T	NP_001341834.1:p.Glu490Asp
NM_001354906.2:c.1101G>T	NP_001341835.1:p.Glu367Asp