Canonical Allele Identifier: CA1573442722
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707784G= , CM000667.2:g.112707784G= GRCh38
NC_000005.9:g.112043481G= , CM000667.1:g.112043481G= GRCh37
NC_000005.8:g.112071380G= NCBI36
NG_008481.4:g.20264G= , LRG_130:g.20264G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000505350.2:c.67G= ENSP00000481752.1:p.Gly23=
ENST00000507379.6:c.67G= ENSP00000423224.2:p.Gly23=
ENST00000509732.6:c.-19+135G= ENSP00000426541.2:n.-19+135G=
ENST00000505350.1:c.67G= ENSP00000481752.1:p.Gly23=
ENST00000507379.5:c.67G= ENSP00000423224.1:p.Gly23=
ENST00000509732.5:c.-19+135G= ENSP00000426541.1:n.-19+135G=
NM_001127511.2:c.67G= NP_001120983.2:p.Gly23=
NM_001354895.1:c.-117G= NP_001341824.1:n.-117G=
NM_001354897.1:c.67G= NP_001341826.1:p.Gly23=
NM_001354902.1:c.67G= NP_001341831.1:p.Gly23=
NM_001127511.3:c.67G= NP_001120983.2:p.Gly23=
NM_001354895.2:c.-117G= NP_001341824.1:n.-117G=
NM_001354897.2:c.67G= NP_001341826.1:p.Gly23=
NM_001354902.2:c.67G= NP_001341831.1:p.Gly23=