Canonical Allele Identifier: CA446206595

Gene: APC

Linked Data

• dbSNP Id: rs2149917865
• MyVariant Identifiers: chr5:g.112175863A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840166A>T , CM000667.2:g.112840166A>T	GRCh38
NC_000005.9:g.112175863A>T , CM000667.1:g.112175863A>T	GRCh37
NC_000005.8:g.112203762A>T	NCBI36
NG_008481.4:g.152646A>T , LRG_130:g.152646A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000504915.3:c.4626A>T	ENSP00000473355.2:p.Ile1542=
ENST00000505350.2:c.*4578A>T	ENSP00000481752.1:n.*4578A>T
ENST00000507379.6:c.4518A>T	ENSP00000423224.2:p.Ile1506=
ENST00000509732.6:c.4572A>T	ENSP00000426541.2:p.Ile1524=
ENST00000512211.7:c.4572A>T	ENSP00000423828.3:p.Ile1524=
ENST00000257430.9:c.4572A>T MANE Select	ENSP00000257430.4:p.Ile1524=
ENST00000257430.8:c.4572A>T	ENSP00000257430.4:p.Ile1524=
ENST00000508376.6:c.4572A>T	ENSP00000427089.2:p.Ile1524=
ENST00000508624.5:c.*3894A>T	ENSP00000424265.1:n.*3894A>T
ENST00000520401.1:c.230+11194A>T
NM_000038.5:c.4572A>T	NP_000029.2:p.Ile1524=
NM_001127510.2:c.4572A>T	NP_001120982.1:p.Ile1524=
NM_001127511.2:c.4518A>T	NP_001120983.2:p.Ile1506=
NM_001354895.1:c.4572A>T	NP_001341824.1:p.Ile1524=
NM_001354896.1:c.4626A>T	NP_001341825.1:p.Ile1542=
NM_001354897.1:c.4602A>T	NP_001341826.1:p.Ile1534=
NM_001354898.1:c.4497A>T	NP_001341827.1:p.Ile1499=
NM_001354899.1:c.4488A>T	NP_001341828.1:p.Ile1496=
NM_001354900.1:c.4449A>T	NP_001341829.1:p.Ile1483=
NM_001354901.1:c.4395A>T	NP_001341830.1:p.Ile1465=
NM_001354902.1:c.4299A>T	NP_001341831.1:p.Ile1433=
NM_001354903.1:c.4269A>T	NP_001341832.1:p.Ile1423=
NM_001354904.1:c.4194A>T	NP_001341833.1:p.Ile1398=
NM_001354905.1:c.4092A>T	NP_001341834.1:p.Ile1364=
NM_001354906.1:c.3723A>T	NP_001341835.1:p.Ile1241=
NM_000038.6:c.4572A>T MANE Select	NP_000029.2:p.Ile1524=
NM_001127510.3:c.4572A>T	NP_001120982.1:p.Ile1524=
NM_001127511.3:c.4518A>T	NP_001120983.2:p.Ile1506=
NM_001354895.2:c.4572A>T	NP_001341824.1:p.Ile1524=
NM_001354896.2:c.4626A>T	NP_001341825.1:p.Ile1542=
NM_001354897.2:c.4602A>T	NP_001341826.1:p.Ile1534=
NM_001354898.2:c.4497A>T	NP_001341827.1:p.Ile1499=
NM_001354899.2:c.4488A>T	NP_001341828.1:p.Ile1496=
NM_001354900.2:c.4449A>T	NP_001341829.1:p.Ile1483=
NM_001354901.2:c.4395A>T	NP_001341830.1:p.Ile1465=
NM_001354902.2:c.4299A>T	NP_001341831.1:p.Ile1433=
NM_001354903.2:c.4269A>T	NP_001341832.1:p.Ile1423=
NM_001354904.2:c.4194A>T	NP_001341833.1:p.Ile1398=
NM_001354905.2:c.4092A>T	NP_001341834.1:p.Ile1364=
NM_001354906.2:c.3723A>T	NP_001341835.1:p.Ile1241=