Canonical Allele Identifier: CA1573484991
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112815575A= , CM000667.2:g.112815575A= GRCh38
NC_000005.9:g.112151272A= , CM000667.1:g.112151272A= GRCh37
NC_000005.8:g.112179171A= NCBI36
NG_008481.4:g.128055A= , LRG_130:g.128055A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000502371.3:c.915A= ENSP00000484935.2:p.Thr305=
ENST00000504915.3:c.915A= ENSP00000473355.2:p.Thr305=
ENST00000505084.2:n.971A=
ENST00000505350.2:c.*921A= ENSP00000481752.1:n.*921A=
ENST00000507379.6:c.861A= ENSP00000423224.2:p.Thr287=
ENST00000509732.6:c.915A= ENSP00000426541.2:p.Thr305=
ENST00000512211.7:c.915A= ENSP00000423828.3:p.Thr305=
ENST00000257430.9:c.915A= MANE Select ENSP00000257430.4:p.Thr305=
ENST00000257430.8:c.915A= ENSP00000257430.4:p.Thr305=
ENST00000507379.5:c.861A= ENSP00000423224.1:p.Thr287=
ENST00000508376.6:c.915A= ENSP00000427089.2:p.Thr305=
ENST00000508624.5:c.*237A= ENSP00000424265.1:n.*237A=
ENST00000512211.6:c.915A= ENSP00000423828.2:p.Thr305=
NM_000038.5:c.915A= NP_000029.2:p.Thr305=
NM_001127510.2:c.915A= NP_001120982.1:p.Thr305=
NM_001127511.2:c.861A= NP_001120983.2:p.Thr287=
NM_001354895.1:c.915A= NP_001341824.1:p.Thr305=
NM_001354896.1:c.915A= NP_001341825.1:p.Thr305=
NM_001354897.1:c.945A= NP_001341826.1:p.Thr315=
NM_001354898.1:c.840A= NP_001341827.1:p.Thr280=
NM_001354899.1:c.831A= NP_001341828.1:p.Thr277=
NM_001354900.1:c.738A= NP_001341829.1:p.Thr246=
NM_001354901.1:c.738A= NP_001341830.1:p.Thr246=
NM_001354902.1:c.945A= NP_001341831.1:p.Thr315=
NM_001354903.1:c.915A= NP_001341832.1:p.Thr305=
NM_001354904.1:c.840A= NP_001341833.1:p.Thr280=
NM_001354905.1:c.738A= NP_001341834.1:p.Thr246=
NM_001354906.1:c.66A= NP_001341835.1:p.Thr22=
NM_000038.6:c.915A= MANE Select NP_000029.2:p.Thr305=
NM_001127510.3:c.915A= NP_001120982.1:p.Thr305=
NM_001127511.3:c.861A= NP_001120983.2:p.Thr287=
NM_001354895.2:c.915A= NP_001341824.1:p.Thr305=
NM_001354896.2:c.915A= NP_001341825.1:p.Thr305=
NM_001354897.2:c.945A= NP_001341826.1:p.Thr315=
NM_001354898.2:c.840A= NP_001341827.1:p.Thr280=
NM_001354899.2:c.831A= NP_001341828.1:p.Thr277=
NM_001354900.2:c.738A= NP_001341829.1:p.Thr246=
NM_001354901.2:c.738A= NP_001341830.1:p.Thr246=
NM_001354902.2:c.945A= NP_001341831.1:p.Thr315=
NM_001354903.2:c.915A= NP_001341832.1:p.Thr305=
NM_001354904.2:c.840A= NP_001341833.1:p.Thr280=
NM_001354905.2:c.738A= NP_001341834.1:p.Thr246=
NM_001354906.2:c.66A= NP_001341835.1:p.Thr22=