Canonical Allele Identifier: CA445963709

Gene: APC

Linked Data

• dbSNP Id: rs876658536
• MyVariant Identifiers: chr5:g.112175098A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839401A>T , CM000667.2:g.112839401A>T	GRCh38
NC_000005.9:g.112175098A>T , CM000667.1:g.112175098A>T	GRCh37
NC_000005.8:g.112202997A>T	NCBI36
NG_008481.4:g.151881A>T , LRG_130:g.151881A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.3472A>T	ENSP00000484935.2:n.3472A>T
ENST00000504915.3:c.3861A>T	ENSP00000473355.2:p.Ile1287=
ENST00000505350.2:c.*3813A>T	ENSP00000481752.1:n.*3813A>T
ENST00000507379.6:c.3753A>T	ENSP00000423224.2:p.Ile1251=
ENST00000509732.6:c.3807A>T	ENSP00000426541.2:p.Ile1269=
ENST00000512211.7:c.3807A>T	ENSP00000423828.3:p.Ile1269=
ENST00000257430.9:c.3807A>T MANE Select	ENSP00000257430.4:p.Ile1269=
ENST00000257430.8:c.3807A>T	ENSP00000257430.4:p.Ile1269=
ENST00000502371.2:c.2160A>T
ENST00000508376.6:c.3807A>T	ENSP00000427089.2:p.Ile1269=
ENST00000508624.5:c.*3129A>T	ENSP00000424265.1:n.*3129A>T
ENST00000512211.6:c.3807A>T	ENSP00000423828.2:p.Ile1269=
ENST00000520401.1:c.230+10429A>T
NM_000038.5:c.3807A>T	NP_000029.2:p.Ile1269=
NM_001127510.2:c.3807A>T	NP_001120982.1:p.Ile1269=
NM_001127511.2:c.3753A>T	NP_001120983.2:p.Ile1251=
NM_001354895.1:c.3807A>T	NP_001341824.1:p.Ile1269=
NM_001354896.1:c.3861A>T	NP_001341825.1:p.Ile1287=
NM_001354897.1:c.3837A>T	NP_001341826.1:p.Ile1279=
NM_001354898.1:c.3732A>T	NP_001341827.1:p.Ile1244=
NM_001354899.1:c.3723A>T	NP_001341828.1:p.Ile1241=
NM_001354900.1:c.3684A>T	NP_001341829.1:p.Ile1228=
NM_001354901.1:c.3630A>T	NP_001341830.1:p.Ile1210=
NM_001354902.1:c.3534A>T	NP_001341831.1:p.Ile1178=
NM_001354903.1:c.3504A>T	NP_001341832.1:p.Ile1168=
NM_001354904.1:c.3429A>T	NP_001341833.1:p.Ile1143=
NM_001354905.1:c.3327A>T	NP_001341834.1:p.Ile1109=
NM_001354906.1:c.2958A>T	NP_001341835.1:p.Ile986=
NM_000038.6:c.3807A>T MANE Select	NP_000029.2:p.Ile1269=
NM_001127510.3:c.3807A>T	NP_001120982.1:p.Ile1269=
NM_001127511.3:c.3753A>T	NP_001120983.2:p.Ile1251=
NM_001354895.2:c.3807A>T	NP_001341824.1:p.Ile1269=
NM_001354896.2:c.3861A>T	NP_001341825.1:p.Ile1287=
NM_001354897.2:c.3837A>T	NP_001341826.1:p.Ile1279=
NM_001354898.2:c.3732A>T	NP_001341827.1:p.Ile1244=
NM_001354899.2:c.3723A>T	NP_001341828.1:p.Ile1241=
NM_001354900.2:c.3684A>T	NP_001341829.1:p.Ile1228=
NM_001354901.2:c.3630A>T	NP_001341830.1:p.Ile1210=
NM_001354902.2:c.3534A>T	NP_001341831.1:p.Ile1178=
NM_001354903.2:c.3504A>T	NP_001341832.1:p.Ile1168=
NM_001354904.2:c.3429A>T	NP_001341833.1:p.Ile1143=
NM_001354905.2:c.3327A>T	NP_001341834.1:p.Ile1109=
NM_001354906.2:c.2958A>T	NP_001341835.1:p.Ile986=