Canonical Allele Identifier: CA16030904

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839964C>T , CM000667.2:g.112839964C>T	GRCh38
NC_000005.9:g.112175661C>T , CM000667.1:g.112175661C>T	GRCh37
NC_000005.8:g.112203560C>T	NCBI36
NG_008481.4:g.152444C>T , LRG_130:g.152444C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000038.6:c.4370C>T MANE Select	NP_000029.2:p.Ala1457Val
ENST00000257430.9:c.4370C>T MANE Select	ENSP00000257430.4:p.Ala1457Val
NM_000038.5:c.4370C>T	NP_000029.2:p.Ala1457Val
NM_001127510.2:c.4370C>T	NP_001120982.1:p.Ala1457Val
NM_001127510.3:c.4370C>T	NP_001120982.1:p.Ala1457Val
NM_001127511.2:c.4316C>T	NP_001120983.2:p.Ala1439Val
NM_001127511.3:c.4316C>T	NP_001120983.2:p.Ala1439Val
NM_001354895.1:c.4370C>T	NP_001341824.1:p.Ala1457Val
NM_001354895.2:c.4370C>T	NP_001341824.1:p.Ala1457Val
NM_001354896.1:c.4424C>T	NP_001341825.1:p.Ala1475Val
NM_001354896.2:c.4424C>T	NP_001341825.1:p.Ala1475Val
NM_001354897.1:c.4400C>T	NP_001341826.1:p.Ala1467Val
NM_001354897.2:c.4400C>T	NP_001341826.1:p.Ala1467Val
NM_001354898.1:c.4295C>T	NP_001341827.1:p.Ala1432Val
NM_001354898.2:c.4295C>T	NP_001341827.1:p.Ala1432Val
NM_001354899.1:c.4286C>T	NP_001341828.1:p.Ala1429Val
NM_001354899.2:c.4286C>T	NP_001341828.1:p.Ala1429Val
NM_001354900.1:c.4247C>T	NP_001341829.1:p.Ala1416Val
NM_001354900.2:c.4247C>T	NP_001341829.1:p.Ala1416Val
NM_001354901.1:c.4193C>T	NP_001341830.1:p.Ala1398Val
NM_001354901.2:c.4193C>T	NP_001341830.1:p.Ala1398Val
NM_001354902.1:c.4097C>T	NP_001341831.1:p.Ala1366Val
NM_001354902.2:c.4097C>T	NP_001341831.1:p.Ala1366Val
NM_001354903.1:c.4067C>T	NP_001341832.1:p.Ala1356Val
NM_001354903.2:c.4067C>T	NP_001341832.1:p.Ala1356Val
NM_001354904.1:c.3992C>T	NP_001341833.1:p.Ala1331Val
NM_001354904.2:c.3992C>T	NP_001341833.1:p.Ala1331Val
NM_001354905.1:c.3890C>T	NP_001341834.1:p.Ala1297Val
NM_001354905.2:c.3890C>T	NP_001341834.1:p.Ala1297Val
NM_001354906.1:c.3521C>T	NP_001341835.1:p.Ala1174Val
NM_001354906.2:c.3521C>T	NP_001341835.1:p.Ala1174Val
ENST00000257430.8:c.4370C>T	ENSP00000257430.4:p.Ala1457Val
ENST00000504915.3:c.4424C>T	ENSP00000473355.2:p.Ala1475Val
ENST00000505350.2:c.*4376C>T	ENSP00000481752.1:n.*4376C>T
ENST00000507379.6:c.4316C>T	ENSP00000423224.2:p.Ala1439Val
ENST00000508376.6:c.4370C>T	ENSP00000427089.2:p.Ala1457Val
ENST00000508624.5:c.*3692C>T	ENSP00000424265.1:n.*3692C>T
ENST00000509732.6:c.4370C>T	ENSP00000426541.2:p.Ala1457Val
ENST00000512211.7:c.4370C>T	ENSP00000423828.3:p.Ala1457Val
ENST00000520401.1:c.230+10992C>T