Canonical Allele Identifier: CA16032096

Gene: APC

Linked Data

• dbSNP Id: rs201797422
• MyVariant Identifiers: chr5:g.112176204T>G (hg19) ; chr5:g.112840507T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840507T>G , CM000667.2:g.112840507T>G	GRCh38
NC_000005.9:g.112176204T>G , CM000667.1:g.112176204T>G	GRCh37
NC_000005.8:g.112204103T>G	NCBI36
NG_008481.4:g.152987T>G , LRG_130:g.152987T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.4967T>G	ENSP00000473355.2:p.Met1656Arg
ENST00000505350.2:c.*4919T>G	ENSP00000481752.1:n.*4919T>G
ENST00000507379.6:c.4859T>G	ENSP00000423224.2:p.Met1620Arg
ENST00000509732.6:c.4913T>G	ENSP00000426541.2:p.Met1638Arg
ENST00000512211.7:c.4913T>G	ENSP00000423828.3:p.Met1638Arg
ENST00000257430.9:c.4913T>G MANE Select	ENSP00000257430.4:p.Met1638Arg
ENST00000257430.8:c.4913T>G	ENSP00000257430.4:p.Met1638Arg
ENST00000508376.6:c.4913T>G	ENSP00000427089.2:p.Met1638Arg
ENST00000508624.5:c.*4235T>G	ENSP00000424265.1:n.*4235T>G
ENST00000520401.1:c.230+11535T>G
NM_000038.5:c.4913T>G	NP_000029.2:p.Met1638Arg
NM_001127510.2:c.4913T>G	NP_001120982.1:p.Met1638Arg
NM_001127511.2:c.4859T>G	NP_001120983.2:p.Met1620Arg
NM_001354895.1:c.4913T>G	NP_001341824.1:p.Met1638Arg
NM_001354896.1:c.4967T>G	NP_001341825.1:p.Met1656Arg
NM_001354897.1:c.4943T>G	NP_001341826.1:p.Met1648Arg
NM_001354898.1:c.4838T>G	NP_001341827.1:p.Met1613Arg
NM_001354899.1:c.4829T>G	NP_001341828.1:p.Met1610Arg
NM_001354900.1:c.4790T>G	NP_001341829.1:p.Met1597Arg
NM_001354901.1:c.4736T>G	NP_001341830.1:p.Met1579Arg
NM_001354902.1:c.4640T>G	NP_001341831.1:p.Met1547Arg
NM_001354903.1:c.4610T>G	NP_001341832.1:p.Met1537Arg
NM_001354904.1:c.4535T>G	NP_001341833.1:p.Met1512Arg
NM_001354905.1:c.4433T>G	NP_001341834.1:p.Met1478Arg
NM_001354906.1:c.4064T>G	NP_001341835.1:p.Met1355Arg
NM_000038.6:c.4913T>G MANE Select	NP_000029.2:p.Met1638Arg
NM_001127510.3:c.4913T>G	NP_001120982.1:p.Met1638Arg
NM_001127511.3:c.4859T>G	NP_001120983.2:p.Met1620Arg
NM_001354895.2:c.4913T>G	NP_001341824.1:p.Met1638Arg
NM_001354896.2:c.4967T>G	NP_001341825.1:p.Met1656Arg
NM_001354897.2:c.4943T>G	NP_001341826.1:p.Met1648Arg
NM_001354898.2:c.4838T>G	NP_001341827.1:p.Met1613Arg
NM_001354899.2:c.4829T>G	NP_001341828.1:p.Met1610Arg
NM_001354900.2:c.4790T>G	NP_001341829.1:p.Met1597Arg
NM_001354901.2:c.4736T>G	NP_001341830.1:p.Met1579Arg
NM_001354902.2:c.4640T>G	NP_001341831.1:p.Met1547Arg
NM_001354903.2:c.4610T>G	NP_001341832.1:p.Met1537Arg
NM_001354904.2:c.4535T>G	NP_001341833.1:p.Met1512Arg
NM_001354905.2:c.4433T>G	NP_001341834.1:p.Met1478Arg
NM_001354906.2:c.4064T>G	NP_001341835.1:p.Met1355Arg