Canonical Allele Identifier: CA16024912

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112164575A>G (hg19) ; chr5:g.112828878A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828878A>G , CM000667.2:g.112828878A>G	GRCh38
NC_000005.9:g.112164575A>G , CM000667.1:g.112164575A>G	GRCh37
NC_000005.8:g.112192474A>G	NCBI36
NG_008481.4:g.141358A>G , LRG_130:g.141358A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1409-6073A>G	ENSP00000484935.2:n.1409-6073A>G
ENST00000504915.3:c.1703A>G	ENSP00000473355.2:p.Asn568Ser
ENST00000505084.2:n.1705A>G
ENST00000505350.2:c.*1655A>G	ENSP00000481752.1:n.*1655A>G
ENST00000507379.6:c.1595A>G	ENSP00000423224.2:p.Asn532Ser
ENST00000509732.6:c.1649A>G	ENSP00000426541.2:p.Asn550Ser
ENST00000512211.7:c.1649A>G	ENSP00000423828.3:p.Asn550Ser
ENST00000257430.9:c.1649A>G MANE Select	ENSP00000257430.4:p.Asn550Ser
ENST00000257430.8:c.1649A>G	ENSP00000257430.4:p.Asn550Ser
ENST00000502371.2:c.97-6073A>G
ENST00000504915.2:c.338A>G	ENSP00000473355.1:p.Asn113Ser
ENST00000505084.1:n.136A>G
ENST00000507379.5:c.1595A>G	ENSP00000423224.1:p.Asn532Ser
ENST00000508376.6:c.1649A>G	ENSP00000427089.2:p.Asn550Ser
ENST00000508624.5:c.*971A>G	ENSP00000424265.1:n.*971A>G
ENST00000512211.6:c.1649A>G	ENSP00000423828.2:p.Asn550Ser
ENST00000520401.1:c.136A>G
NM_000038.5:c.1649A>G	NP_000029.2:p.Asn550Ser
NM_001127510.2:c.1649A>G	NP_001120982.1:p.Asn550Ser
NM_001127511.2:c.1595A>G	NP_001120983.2:p.Asn532Ser
NM_001354895.1:c.1649A>G	NP_001341824.1:p.Asn550Ser
NM_001354896.1:c.1703A>G	NP_001341825.1:p.Asn568Ser
NM_001354897.1:c.1679A>G	NP_001341826.1:p.Asn560Ser
NM_001354898.1:c.1574A>G	NP_001341827.1:p.Asn525Ser
NM_001354899.1:c.1565A>G	NP_001341828.1:p.Asn522Ser
NM_001354900.1:c.1526A>G	NP_001341829.1:p.Asn509Ser
NM_001354901.1:c.1472A>G	NP_001341830.1:p.Asn491Ser
NM_001354902.1:c.1376A>G	NP_001341831.1:p.Asn459Ser
NM_001354903.1:c.1346A>G	NP_001341832.1:p.Asn449Ser
NM_001354904.1:c.1271A>G	NP_001341833.1:p.Asn424Ser
NM_001354905.1:c.1169A>G	NP_001341834.1:p.Asn390Ser
NM_001354906.1:c.800A>G	NP_001341835.1:p.Asn267Ser
NM_000038.6:c.1649A>G MANE Select	NP_000029.2:p.Asn550Ser
NM_001127510.3:c.1649A>G	NP_001120982.1:p.Asn550Ser
NM_001127511.3:c.1595A>G	NP_001120983.2:p.Asn532Ser
NM_001354895.2:c.1649A>G	NP_001341824.1:p.Asn550Ser
NM_001354896.2:c.1703A>G	NP_001341825.1:p.Asn568Ser
NM_001354897.2:c.1679A>G	NP_001341826.1:p.Asn560Ser
NM_001354898.2:c.1574A>G	NP_001341827.1:p.Asn525Ser
NM_001354899.2:c.1565A>G	NP_001341828.1:p.Asn522Ser
NM_001354900.2:c.1526A>G	NP_001341829.1:p.Asn509Ser
NM_001354901.2:c.1472A>G	NP_001341830.1:p.Asn491Ser
NM_001354902.2:c.1376A>G	NP_001341831.1:p.Asn459Ser
NM_001354903.2:c.1346A>G	NP_001341832.1:p.Asn449Ser
NM_001354904.2:c.1271A>G	NP_001341833.1:p.Asn424Ser
NM_001354905.2:c.1169A>G	NP_001341834.1:p.Asn390Ser
NM_001354906.2:c.800A>G	NP_001341835.1:p.Asn267Ser