Canonical Allele Identifier: CA446211062

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843679A>G , CM000667.2:g.112843679A>G	GRCh38
NC_000005.9:g.112179376A>G , CM000667.1:g.112179376A>G	GRCh37
NC_000005.8:g.112207275A>G	NCBI36
NG_008481.4:g.156159A>G , LRG_130:g.156159A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000038.6:c.8085A>G MANE Select	NP_000029.2:p.Lys2695=
ENST00000257430.9:c.8085A>G MANE Select	ENSP00000257430.4:p.Lys2695=
NM_000038.5:c.8085A>G	NP_000029.2:p.Lys2695=
NM_001127510.2:c.8085A>G	NP_001120982.1:p.Lys2695=
NM_001127510.3:c.8085A>G	NP_001120982.1:p.Lys2695=
NM_001127511.2:c.8031A>G	NP_001120983.2:p.Lys2677=
NM_001127511.3:c.8031A>G	NP_001120983.2:p.Lys2677=
NM_001354895.1:c.8085A>G	NP_001341824.1:p.Lys2695=
NM_001354895.2:c.8085A>G	NP_001341824.1:p.Lys2695=
NM_001354896.1:c.8139A>G	NP_001341825.1:p.Lys2713=
NM_001354896.2:c.8139A>G	NP_001341825.1:p.Lys2713=
NM_001354897.1:c.8115A>G	NP_001341826.1:p.Lys2705=
NM_001354897.2:c.8115A>G	NP_001341826.1:p.Lys2705=
NM_001354898.1:c.8010A>G	NP_001341827.1:p.Lys2670=
NM_001354898.2:c.8010A>G	NP_001341827.1:p.Lys2670=
NM_001354899.1:c.8001A>G	NP_001341828.1:p.Lys2667=
NM_001354899.2:c.8001A>G	NP_001341828.1:p.Lys2667=
NM_001354900.1:c.7962A>G	NP_001341829.1:p.Lys2654=
NM_001354900.2:c.7962A>G	NP_001341829.1:p.Lys2654=
NM_001354901.1:c.7908A>G	NP_001341830.1:p.Lys2636=
NM_001354901.2:c.7908A>G	NP_001341830.1:p.Lys2636=
NM_001354902.1:c.7812A>G	NP_001341831.1:p.Lys2604=
NM_001354902.2:c.7812A>G	NP_001341831.1:p.Lys2604=
NM_001354903.1:c.7782A>G	NP_001341832.1:p.Lys2594=
NM_001354903.2:c.7782A>G	NP_001341832.1:p.Lys2594=
NM_001354904.1:c.7707A>G	NP_001341833.1:p.Lys2569=
NM_001354904.2:c.7707A>G	NP_001341833.1:p.Lys2569=
NM_001354905.1:c.7605A>G	NP_001341834.1:p.Lys2535=
NM_001354905.2:c.7605A>G	NP_001341834.1:p.Lys2535=
NM_001354906.1:c.7236A>G	NP_001341835.1:p.Lys2412=
NM_001354906.2:c.7236A>G	NP_001341835.1:p.Lys2412=
ENST00000257430.8:c.8085A>G	ENSP00000257430.4:p.Lys2695=
ENST00000504915.3:c.8139A>G	ENSP00000473355.2:p.Lys2713=
ENST00000505350.2:c.*8091A>G	ENSP00000481752.1:n.*8091A>G
ENST00000507379.6:c.8031A>G	ENSP00000423224.2:p.Lys2677=
ENST00000508376.6:c.8085A>G	ENSP00000427089.2:p.Lys2695=
ENST00000509732.6:c.8085A>G	ENSP00000426541.2:p.Lys2695=
ENST00000512211.7:c.8085A>G	ENSP00000423828.3:p.Lys2695=
ENST00000520401.1:c.231-12970A>G