Canonical Allele Identifier: CA16024887

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112164564T>G (hg19) ; chr5:g.112828867T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828867T>G , CM000667.2:g.112828867T>G	GRCh38
NC_000005.9:g.112164564T>G , CM000667.1:g.112164564T>G	GRCh37
NC_000005.8:g.112192463T>G	NCBI36
NG_008481.4:g.141347T>G , LRG_130:g.141347T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1409-6084T>G	ENSP00000484935.2:n.1409-6084T>G
ENST00000504915.3:c.1692T>G	ENSP00000473355.2:p.Ser564Arg
ENST00000505084.2:n.1694T>G
ENST00000505350.2:c.*1644T>G	ENSP00000481752.1:n.*1644T>G
ENST00000507379.6:c.1584T>G	ENSP00000423224.2:p.Ser528Arg
ENST00000509732.6:c.1638T>G	ENSP00000426541.2:p.Ser546Arg
ENST00000512211.7:c.1638T>G	ENSP00000423828.3:p.Ser546Arg
ENST00000257430.9:c.1638T>G MANE Select	ENSP00000257430.4:p.Ser546Arg
ENST00000257430.8:c.1638T>G	ENSP00000257430.4:p.Ser546Arg
ENST00000502371.2:c.97-6084T>G
ENST00000504915.2:c.327T>G	ENSP00000473355.1:p.Ser109Arg
ENST00000505084.1:n.125T>G
ENST00000507379.5:c.1584T>G	ENSP00000423224.1:p.Ser528Arg
ENST00000508376.6:c.1638T>G	ENSP00000427089.2:p.Ser546Arg
ENST00000508624.5:c.*960T>G	ENSP00000424265.1:n.*960T>G
ENST00000512211.6:c.1638T>G	ENSP00000423828.2:p.Ser546Arg
ENST00000520401.1:c.125T>G
NM_000038.5:c.1638T>G	NP_000029.2:p.Ser546Arg
NM_001127510.2:c.1638T>G	NP_001120982.1:p.Ser546Arg
NM_001127511.2:c.1584T>G	NP_001120983.2:p.Ser528Arg
NM_001354895.1:c.1638T>G	NP_001341824.1:p.Ser546Arg
NM_001354896.1:c.1692T>G	NP_001341825.1:p.Ser564Arg
NM_001354897.1:c.1668T>G	NP_001341826.1:p.Ser556Arg
NM_001354898.1:c.1563T>G	NP_001341827.1:p.Ser521Arg
NM_001354899.1:c.1554T>G	NP_001341828.1:p.Ser518Arg
NM_001354900.1:c.1515T>G	NP_001341829.1:p.Ser505Arg
NM_001354901.1:c.1461T>G	NP_001341830.1:p.Ser487Arg
NM_001354902.1:c.1365T>G	NP_001341831.1:p.Ser455Arg
NM_001354903.1:c.1335T>G	NP_001341832.1:p.Ser445Arg
NM_001354904.1:c.1260T>G	NP_001341833.1:p.Ser420Arg
NM_001354905.1:c.1158T>G	NP_001341834.1:p.Ser386Arg
NM_001354906.1:c.789T>G	NP_001341835.1:p.Ser263Arg
NM_000038.6:c.1638T>G MANE Select	NP_000029.2:p.Ser546Arg
NM_001127510.3:c.1638T>G	NP_001120982.1:p.Ser546Arg
NM_001127511.3:c.1584T>G	NP_001120983.2:p.Ser528Arg
NM_001354895.2:c.1638T>G	NP_001341824.1:p.Ser546Arg
NM_001354896.2:c.1692T>G	NP_001341825.1:p.Ser564Arg
NM_001354897.2:c.1668T>G	NP_001341826.1:p.Ser556Arg
NM_001354898.2:c.1563T>G	NP_001341827.1:p.Ser521Arg
NM_001354899.2:c.1554T>G	NP_001341828.1:p.Ser518Arg
NM_001354900.2:c.1515T>G	NP_001341829.1:p.Ser505Arg
NM_001354901.2:c.1461T>G	NP_001341830.1:p.Ser487Arg
NM_001354902.2:c.1365T>G	NP_001341831.1:p.Ser455Arg
NM_001354903.2:c.1335T>G	NP_001341832.1:p.Ser445Arg
NM_001354904.2:c.1260T>G	NP_001341833.1:p.Ser420Arg
NM_001354905.2:c.1158T>G	NP_001341834.1:p.Ser386Arg
NM_001354906.2:c.789T>G	NP_001341835.1:p.Ser263Arg