Canonical Allele Identifier: CA16024898

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112164569T>G (hg19) ; chr5:g.112828872T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112828872T>G , CM000667.2:g.112828872T>G	GRCh38
NC_000005.9:g.112164569T>G , CM000667.1:g.112164569T>G	GRCh37
NC_000005.8:g.112192468T>G	NCBI36
NG_008481.4:g.141352T>G , LRG_130:g.141352T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1409-6079T>G	ENSP00000484935.2:n.1409-6079T>G
ENST00000504915.3:c.1697T>G	ENSP00000473355.2:p.Leu566Trp
ENST00000505084.2:n.1699T>G
ENST00000505350.2:c.*1649T>G	ENSP00000481752.1:n.*1649T>G
ENST00000507379.6:c.1589T>G	ENSP00000423224.2:p.Leu530Trp
ENST00000509732.6:c.1643T>G	ENSP00000426541.2:p.Leu548Trp
ENST00000512211.7:c.1643T>G	ENSP00000423828.3:p.Leu548Trp
ENST00000257430.9:c.1643T>G MANE Select	ENSP00000257430.4:p.Leu548Trp
ENST00000257430.8:c.1643T>G	ENSP00000257430.4:p.Leu548Trp
ENST00000502371.2:c.97-6079T>G
ENST00000504915.2:c.332T>G	ENSP00000473355.1:p.Leu111Trp
ENST00000505084.1:n.130T>G
ENST00000507379.5:c.1589T>G	ENSP00000423224.1:p.Leu530Trp
ENST00000508376.6:c.1643T>G	ENSP00000427089.2:p.Leu548Trp
ENST00000508624.5:c.*965T>G	ENSP00000424265.1:n.*965T>G
ENST00000512211.6:c.1643T>G	ENSP00000423828.2:p.Leu548Trp
ENST00000520401.1:c.130T>G
NM_000038.5:c.1643T>G	NP_000029.2:p.Leu548Trp
NM_001127510.2:c.1643T>G	NP_001120982.1:p.Leu548Trp
NM_001127511.2:c.1589T>G	NP_001120983.2:p.Leu530Trp
NM_001354895.1:c.1643T>G	NP_001341824.1:p.Leu548Trp
NM_001354896.1:c.1697T>G	NP_001341825.1:p.Leu566Trp
NM_001354897.1:c.1673T>G	NP_001341826.1:p.Leu558Trp
NM_001354898.1:c.1568T>G	NP_001341827.1:p.Leu523Trp
NM_001354899.1:c.1559T>G	NP_001341828.1:p.Leu520Trp
NM_001354900.1:c.1520T>G	NP_001341829.1:p.Leu507Trp
NM_001354901.1:c.1466T>G	NP_001341830.1:p.Leu489Trp
NM_001354902.1:c.1370T>G	NP_001341831.1:p.Leu457Trp
NM_001354903.1:c.1340T>G	NP_001341832.1:p.Leu447Trp
NM_001354904.1:c.1265T>G	NP_001341833.1:p.Leu422Trp
NM_001354905.1:c.1163T>G	NP_001341834.1:p.Leu388Trp
NM_001354906.1:c.794T>G	NP_001341835.1:p.Leu265Trp
NM_000038.6:c.1643T>G MANE Select	NP_000029.2:p.Leu548Trp
NM_001127510.3:c.1643T>G	NP_001120982.1:p.Leu548Trp
NM_001127511.3:c.1589T>G	NP_001120983.2:p.Leu530Trp
NM_001354895.2:c.1643T>G	NP_001341824.1:p.Leu548Trp
NM_001354896.2:c.1697T>G	NP_001341825.1:p.Leu566Trp
NM_001354897.2:c.1673T>G	NP_001341826.1:p.Leu558Trp
NM_001354898.2:c.1568T>G	NP_001341827.1:p.Leu523Trp
NM_001354899.2:c.1559T>G	NP_001341828.1:p.Leu520Trp
NM_001354900.2:c.1520T>G	NP_001341829.1:p.Leu507Trp
NM_001354901.2:c.1466T>G	NP_001341830.1:p.Leu489Trp
NM_001354902.2:c.1370T>G	NP_001341831.1:p.Leu457Trp
NM_001354903.2:c.1340T>G	NP_001341832.1:p.Leu447Trp
NM_001354904.2:c.1265T>G	NP_001341833.1:p.Leu422Trp
NM_001354905.2:c.1163T>G	NP_001341834.1:p.Leu388Trp
NM_001354906.2:c.794T>G	NP_001341835.1:p.Leu265Trp