Canonical Allele Identifier: CA446210826

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112178353T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112842656T>G , CM000667.2:g.112842656T>G	GRCh38
NC_000005.9:g.112178353T>G , CM000667.1:g.112178353T>G	GRCh37
NC_000005.8:g.112206252T>G	NCBI36
NG_008481.4:g.155136T>G , LRG_130:g.155136T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7116T>G	ENSP00000473355.2:p.Ala2372=
ENST00000505350.2:c.*7068T>G	ENSP00000481752.1:n.*7068T>G
ENST00000507379.6:c.7008T>G	ENSP00000423224.2:p.Ala2336=
ENST00000509732.6:c.7062T>G	ENSP00000426541.2:p.Ala2354=
ENST00000512211.7:c.7062T>G	ENSP00000423828.3:p.Ala2354=
ENST00000257430.9:c.7062T>G MANE Select	ENSP00000257430.4:p.Ala2354=
ENST00000257430.8:c.7062T>G	ENSP00000257430.4:p.Ala2354=
ENST00000508376.6:c.7062T>G	ENSP00000427089.2:p.Ala2354=
ENST00000508624.5:c.*6384T>G	ENSP00000424265.1:n.*6384T>G
ENST00000520401.1:c.230+13684T>G
NM_000038.5:c.7062T>G	NP_000029.2:p.Ala2354=
NM_001127510.2:c.7062T>G	NP_001120982.1:p.Ala2354=
NM_001127511.2:c.7008T>G	NP_001120983.2:p.Ala2336=
NM_001354895.1:c.7062T>G	NP_001341824.1:p.Ala2354=
NM_001354896.1:c.7116T>G	NP_001341825.1:p.Ala2372=
NM_001354897.1:c.7092T>G	NP_001341826.1:p.Ala2364=
NM_001354898.1:c.6987T>G	NP_001341827.1:p.Ala2329=
NM_001354899.1:c.6978T>G	NP_001341828.1:p.Ala2326=
NM_001354900.1:c.6939T>G	NP_001341829.1:p.Ala2313=
NM_001354901.1:c.6885T>G	NP_001341830.1:p.Ala2295=
NM_001354902.1:c.6789T>G	NP_001341831.1:p.Ala2263=
NM_001354903.1:c.6759T>G	NP_001341832.1:p.Ala2253=
NM_001354904.1:c.6684T>G	NP_001341833.1:p.Ala2228=
NM_001354905.1:c.6582T>G	NP_001341834.1:p.Ala2194=
NM_001354906.1:c.6213T>G	NP_001341835.1:p.Ala2071=
NM_000038.6:c.7062T>G MANE Select	NP_000029.2:p.Ala2354=
NM_001127510.3:c.7062T>G	NP_001120982.1:p.Ala2354=
NM_001127511.3:c.7008T>G	NP_001120983.2:p.Ala2336=
NM_001354895.2:c.7062T>G	NP_001341824.1:p.Ala2354=
NM_001354896.2:c.7116T>G	NP_001341825.1:p.Ala2372=
NM_001354897.2:c.7092T>G	NP_001341826.1:p.Ala2364=
NM_001354898.2:c.6987T>G	NP_001341827.1:p.Ala2329=
NM_001354899.2:c.6978T>G	NP_001341828.1:p.Ala2326=
NM_001354900.2:c.6939T>G	NP_001341829.1:p.Ala2313=
NM_001354901.2:c.6885T>G	NP_001341830.1:p.Ala2295=
NM_001354902.2:c.6789T>G	NP_001341831.1:p.Ala2263=
NM_001354903.2:c.6759T>G	NP_001341832.1:p.Ala2253=
NM_001354904.2:c.6684T>G	NP_001341833.1:p.Ala2228=
NM_001354905.2:c.6582T>G	NP_001341834.1:p.Ala2194=
NM_001354906.2:c.6213T>G	NP_001341835.1:p.Ala2071=