Canonical Allele Identifier: CA1573458304
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112737428A= , CM000667.2:g.112737428A= GRCh38
NC_000005.9:g.112073125A= , CM000667.1:g.112073125A= GRCh37
NC_000005.8:g.112101024A= NCBI36
NG_008481.4:g.49908A= , LRG_130:g.49908A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000505350.2:c.166-17445A= ENSP00000481752.1:n.166-17445A=
ENST00000507379.6:c.166-28898A= ENSP00000423224.2:n.166-28898A=
ENST00000509732.6:c.-18-17445A= ENSP00000426541.2:n.-18-17445A=
ENST00000505350.1:c.166-17445A= ENSP00000481752.1:n.166-17445A=
ENST00000507379.5:c.166-28898A= ENSP00000423224.1:n.166-28898A=
ENST00000509732.5:c.-18-17445A= ENSP00000426541.1:n.-18-17445A=
NM_001127511.2:c.166-28898A= NP_001120983.2:n.166-28898A=
NM_001354895.1:c.-18-17445A= NP_001341824.1:n.-18-17445A=
NM_001354897.1:c.166-28898A= NP_001341826.1:n.166-28898A=
NM_001354902.1:c.166-28898A= NP_001341831.1:n.166-28898A=
NM_001127511.3:c.166-28898A= NP_001120983.2:n.166-28898A=
NM_001354895.2:c.-18-17445A= NP_001341824.1:n.-18-17445A=
NM_001354897.2:c.166-28898A= NP_001341826.1:n.166-28898A=
NM_001354902.2:c.166-28898A= NP_001341831.1:n.166-28898A=