Canonical Allele Identifier: CA446210896

Gene: APC

Linked Data

• ClinVar Variation Id: 1759531
• ClinVar RCV Id: RCV002394031
• MyVariant Identifiers: chr5:g.112178854A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843157A>G , CM000667.2:g.112843157A>G	GRCh38
NC_000005.9:g.112178854A>G , CM000667.1:g.112178854A>G	GRCh37
NC_000005.8:g.112206753A>G	NCBI36
NG_008481.4:g.155637A>G , LRG_130:g.155637A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7617A>G	ENSP00000473355.2:p.Arg2539=
ENST00000505350.2:c.*7569A>G	ENSP00000481752.1:n.*7569A>G
ENST00000507379.6:c.7509A>G	ENSP00000423224.2:p.Arg2503=
ENST00000509732.6:c.7563A>G	ENSP00000426541.2:p.Arg2521=
ENST00000512211.7:c.7563A>G	ENSP00000423828.3:p.Arg2521=
ENST00000257430.9:c.7563A>G MANE Select	ENSP00000257430.4:p.Arg2521=
ENST00000257430.8:c.7563A>G	ENSP00000257430.4:p.Arg2521=
ENST00000508376.6:c.7563A>G	ENSP00000427089.2:p.Arg2521=
ENST00000520401.1:c.231-13492A>G
NM_000038.5:c.7563A>G	NP_000029.2:p.Arg2521=
NM_001127510.2:c.7563A>G	NP_001120982.1:p.Arg2521=
NM_001127511.2:c.7509A>G	NP_001120983.2:p.Arg2503=
NM_001354895.1:c.7563A>G	NP_001341824.1:p.Arg2521=
NM_001354896.1:c.7617A>G	NP_001341825.1:p.Arg2539=
NM_001354897.1:c.7593A>G	NP_001341826.1:p.Arg2531=
NM_001354898.1:c.7488A>G	NP_001341827.1:p.Arg2496=
NM_001354899.1:c.7479A>G	NP_001341828.1:p.Arg2493=
NM_001354900.1:c.7440A>G	NP_001341829.1:p.Arg2480=
NM_001354901.1:c.7386A>G	NP_001341830.1:p.Arg2462=
NM_001354902.1:c.7290A>G	NP_001341831.1:p.Arg2430=
NM_001354903.1:c.7260A>G	NP_001341832.1:p.Arg2420=
NM_001354904.1:c.7185A>G	NP_001341833.1:p.Arg2395=
NM_001354905.1:c.7083A>G	NP_001341834.1:p.Arg2361=
NM_001354906.1:c.6714A>G	NP_001341835.1:p.Arg2238=
NM_000038.6:c.7563A>G MANE Select	NP_000029.2:p.Arg2521=
NM_001127510.3:c.7563A>G	NP_001120982.1:p.Arg2521=
NM_001127511.3:c.7509A>G	NP_001120983.2:p.Arg2503=
NM_001354895.2:c.7563A>G	NP_001341824.1:p.Arg2521=
NM_001354896.2:c.7617A>G	NP_001341825.1:p.Arg2539=
NM_001354897.2:c.7593A>G	NP_001341826.1:p.Arg2531=
NM_001354898.2:c.7488A>G	NP_001341827.1:p.Arg2496=
NM_001354899.2:c.7479A>G	NP_001341828.1:p.Arg2493=
NM_001354900.2:c.7440A>G	NP_001341829.1:p.Arg2480=
NM_001354901.2:c.7386A>G	NP_001341830.1:p.Arg2462=
NM_001354902.2:c.7290A>G	NP_001341831.1:p.Arg2430=
NM_001354903.2:c.7260A>G	NP_001341832.1:p.Arg2420=
NM_001354904.2:c.7185A>G	NP_001341833.1:p.Arg2395=
NM_001354905.2:c.7083A>G	NP_001341834.1:p.Arg2361=
NM_001354906.2:c.6714A>G	NP_001341835.1:p.Arg2238=