Canonical Allele Identifier: CA445963674
Gene: APC HGNC NCBI

Linked Data

dbSNP Id: rs2149890386
MyVariant Identifiers: chr5:g.112174654T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112838957T>A , CM000667.2:g.112838957T>A GRCh38
NC_000005.9:g.112174654T>A , CM000667.1:g.112174654T>A GRCh37
NC_000005.8:g.112202553T>A NCBI36
NG_008481.4:g.151437T>A , LRG_130:g.151437T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000502371.3:c.3028T>A ENSP00000484935.2:n.3028T>A
ENST00000504915.3:c.3417T>A ENSP00000473355.2:p.Ile1139=
ENST00000505350.2:c.*3369T>A ENSP00000481752.1:n.*3369T>A
ENST00000507379.6:c.3309T>A ENSP00000423224.2:p.Ile1103=
ENST00000509732.6:c.3363T>A ENSP00000426541.2:p.Ile1121=
ENST00000512211.7:c.3363T>A ENSP00000423828.3:p.Ile1121=
ENST00000257430.9:c.3363T>A MANE Select ENSP00000257430.4:p.Ile1121=
ENST00000257430.8:c.3363T>A ENSP00000257430.4:p.Ile1121=
ENST00000502371.2:c.1716T>A
ENST00000507379.5:c.3309T>A ENSP00000423224.1:p.Ile1103=
ENST00000508376.6:c.3363T>A ENSP00000427089.2:p.Ile1121=
ENST00000508624.5:c.*2685T>A ENSP00000424265.1:n.*2685T>A
ENST00000512211.6:c.3363T>A ENSP00000423828.2:p.Ile1121=
ENST00000520401.1:c.230+9985T>A
NM_000038.5:c.3363T>A NP_000029.2:p.Ile1121=
NM_001127510.2:c.3363T>A NP_001120982.1:p.Ile1121=
NM_001127511.2:c.3309T>A NP_001120983.2:p.Ile1103=
NM_001354895.1:c.3363T>A NP_001341824.1:p.Ile1121=
NM_001354896.1:c.3417T>A NP_001341825.1:p.Ile1139=
NM_001354897.1:c.3393T>A NP_001341826.1:p.Ile1131=
NM_001354898.1:c.3288T>A NP_001341827.1:p.Ile1096=
NM_001354899.1:c.3279T>A NP_001341828.1:p.Ile1093=
NM_001354900.1:c.3240T>A NP_001341829.1:p.Ile1080=
NM_001354901.1:c.3186T>A NP_001341830.1:p.Ile1062=
NM_001354902.1:c.3090T>A NP_001341831.1:p.Ile1030=
NM_001354903.1:c.3060T>A NP_001341832.1:p.Ile1020=
NM_001354904.1:c.2985T>A NP_001341833.1:p.Ile995=
NM_001354905.1:c.2883T>A NP_001341834.1:p.Ile961=
NM_001354906.1:c.2514T>A NP_001341835.1:p.Ile838=
NM_000038.6:c.3363T>A MANE Select NP_000029.2:p.Ile1121=
NM_001127510.3:c.3363T>A NP_001120982.1:p.Ile1121=
NM_001127511.3:c.3309T>A NP_001120983.2:p.Ile1103=
NM_001354895.2:c.3363T>A NP_001341824.1:p.Ile1121=
NM_001354896.2:c.3417T>A NP_001341825.1:p.Ile1139=
NM_001354897.2:c.3393T>A NP_001341826.1:p.Ile1131=
NM_001354898.2:c.3288T>A NP_001341827.1:p.Ile1096=
NM_001354899.2:c.3279T>A NP_001341828.1:p.Ile1093=
NM_001354900.2:c.3240T>A NP_001341829.1:p.Ile1080=
NM_001354901.2:c.3186T>A NP_001341830.1:p.Ile1062=
NM_001354902.2:c.3090T>A NP_001341831.1:p.Ile1030=
NM_001354903.2:c.3060T>A NP_001341832.1:p.Ile1020=
NM_001354904.2:c.2985T>A NP_001341833.1:p.Ile995=
NM_001354905.2:c.2883T>A NP_001341834.1:p.Ile961=
NM_001354906.2:c.2514T>A NP_001341835.1:p.Ile838=