Canonical Allele Identifier: CA445757390

Gene: APC

Linked Data

• dbSNP Id: rs1057521976
• MyVariant Identifiers: chr5:g.112164588A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828891A>G , CM000667.2:g.112828891A>G	GRCh38
NC_000005.9:g.112164588A>G , CM000667.1:g.112164588A>G	GRCh37
NC_000005.8:g.112192487A>G	NCBI36
NG_008481.4:g.141371A>G , LRG_130:g.141371A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1409-6060A>G	ENSP00000484935.2:n.1409-6060A>G
ENST00000504915.3:c.1716A>G	ENSP00000473355.2:p.Arg572=
ENST00000505084.2:n.1718A>G
ENST00000505350.2:c.*1668A>G	ENSP00000481752.1:n.*1668A>G
ENST00000507379.6:c.1608A>G	ENSP00000423224.2:p.Arg536=
ENST00000509732.6:c.1662A>G	ENSP00000426541.2:p.Arg554=
ENST00000512211.7:c.1662A>G	ENSP00000423828.3:p.Arg554=
ENST00000257430.9:c.1662A>G MANE Select	ENSP00000257430.4:p.Arg554=
ENST00000257430.8:c.1662A>G	ENSP00000257430.4:p.Arg554=
ENST00000502371.2:c.97-6060A>G
ENST00000504915.2:c.351A>G	ENSP00000473355.1:p.Arg117=
ENST00000505084.1:n.149A>G
ENST00000507379.5:c.1608A>G	ENSP00000423224.1:p.Arg536=
ENST00000508376.6:c.1662A>G	ENSP00000427089.2:p.Arg554=
ENST00000508624.5:c.*984A>G	ENSP00000424265.1:n.*984A>G
ENST00000512211.6:c.1662A>G	ENSP00000423828.2:p.Arg554=
ENST00000520401.1:c.149A>G
NM_000038.5:c.1662A>G	NP_000029.2:p.Arg554=
NM_001127510.2:c.1662A>G	NP_001120982.1:p.Arg554=
NM_001127511.2:c.1608A>G	NP_001120983.2:p.Arg536=
NM_001354895.1:c.1662A>G	NP_001341824.1:p.Arg554=
NM_001354896.1:c.1716A>G	NP_001341825.1:p.Arg572=
NM_001354897.1:c.1692A>G	NP_001341826.1:p.Arg564=
NM_001354898.1:c.1587A>G	NP_001341827.1:p.Arg529=
NM_001354899.1:c.1578A>G	NP_001341828.1:p.Arg526=
NM_001354900.1:c.1539A>G	NP_001341829.1:p.Arg513=
NM_001354901.1:c.1485A>G	NP_001341830.1:p.Arg495=
NM_001354902.1:c.1389A>G	NP_001341831.1:p.Arg463=
NM_001354903.1:c.1359A>G	NP_001341832.1:p.Arg453=
NM_001354904.1:c.1284A>G	NP_001341833.1:p.Arg428=
NM_001354905.1:c.1182A>G	NP_001341834.1:p.Arg394=
NM_001354906.1:c.813A>G	NP_001341835.1:p.Arg271=
NM_000038.6:c.1662A>G MANE Select	NP_000029.2:p.Arg554=
NM_001127510.3:c.1662A>G	NP_001120982.1:p.Arg554=
NM_001127511.3:c.1608A>G	NP_001120983.2:p.Arg536=
NM_001354895.2:c.1662A>G	NP_001341824.1:p.Arg554=
NM_001354896.2:c.1716A>G	NP_001341825.1:p.Arg572=
NM_001354897.2:c.1692A>G	NP_001341826.1:p.Arg564=
NM_001354898.2:c.1587A>G	NP_001341827.1:p.Arg529=
NM_001354899.2:c.1578A>G	NP_001341828.1:p.Arg526=
NM_001354900.2:c.1539A>G	NP_001341829.1:p.Arg513=
NM_001354901.2:c.1485A>G	NP_001341830.1:p.Arg495=
NM_001354902.2:c.1389A>G	NP_001341831.1:p.Arg463=
NM_001354903.2:c.1359A>G	NP_001341832.1:p.Arg453=
NM_001354904.2:c.1284A>G	NP_001341833.1:p.Arg428=
NM_001354905.2:c.1182A>G	NP_001341834.1:p.Arg394=
NM_001354906.2:c.813A>G	NP_001341835.1:p.Arg271=