Canonical Allele Identifier: CA1573442458
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707570A= , CM000667.2:g.112707570A= GRCh38
NC_000005.9:g.112043267A= , CM000667.1:g.112043267A= GRCh37
NC_000005.8:g.112071166A= NCBI36
NG_008481.4:g.20050A= , LRG_130:g.20050A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000505350.2:c.-148A= ENSP00000481752.1:n.-148A=
ENST00000507379.6:c.-148A= ENSP00000423224.2:n.-148A=
ENST00000509732.6:c.-98A= ENSP00000426541.2:n.-98A=
ENST00000505350.1:c.-148A= ENSP00000481752.1:n.-148A=
ENST00000507379.5:c.-148A= ENSP00000423224.1:n.-148A=
ENST00000509732.5:c.-98A= ENSP00000426541.1:n.-98A=
NM_001127511.2:c.-148A= NP_001120983.2:n.-148A=
NM_001354895.1:c.-331A= NP_001341824.1:n.-331A=
NM_001354897.1:c.-148A= NP_001341826.1:n.-148A=
NM_001354902.1:c.-148A= NP_001341831.1:n.-148A=
NM_001127511.3:c.-148A= NP_001120983.2:n.-148A=
NM_001354895.2:c.-331A= NP_001341824.1:n.-331A=
NM_001354897.2:c.-148A= NP_001341826.1:n.-148A=
NM_001354902.2:c.-148A= NP_001341831.1:n.-148A=