Canonical Allele Identifier: CA1573442680
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707727T= , CM000667.2:g.112707727T= GRCh38
NC_000005.9:g.112043424T= , CM000667.1:g.112043424T= GRCh37
NC_000005.8:g.112071323T= NCBI36
NG_008481.4:g.20207T= , LRG_130:g.20207T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000505350.2:c.10T= ENSP00000481752.1:p.Ser4=
ENST00000507379.6:c.10T= ENSP00000423224.2:p.Ser4=
ENST00000509732.6:c.-19+78T= ENSP00000426541.2:n.-19+78T=
ENST00000505350.1:c.10T= ENSP00000481752.1:p.Ser4=
ENST00000507379.5:c.10T= ENSP00000423224.1:p.Ser4=
ENST00000509732.5:c.-19+78T= ENSP00000426541.1:n.-19+78T=
NM_001127511.2:c.10T= NP_001120983.2:p.Ser4=
NM_001354895.1:c.-174T= NP_001341824.1:n.-174T=
NM_001354897.1:c.10T= NP_001341826.1:p.Ser4=
NM_001354902.1:c.10T= NP_001341831.1:p.Ser4=
NM_001127511.3:c.10T= NP_001120983.2:p.Ser4=
NM_001354895.2:c.-174T= NP_001341824.1:n.-174T=
NM_001354897.2:c.10T= NP_001341826.1:p.Ser4=
NM_001354902.2:c.10T= NP_001341831.1:p.Ser4=