Canonical Allele Identifier: CA1573458278

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112737398T= , CM000667.2:g.112737398T=	GRCh38
NC_000005.9:g.112073095T= , CM000667.1:g.112073095T=	GRCh37
NC_000005.8:g.112100994T=	NCBI36
NG_008481.4:g.49878T= , LRG_130:g.49878T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.166-17475T=	ENSP00000481752.1:n.166-17475T=
ENST00000507379.6:c.166-28928T=	ENSP00000423224.2:n.166-28928T=
ENST00000509732.6:c.-18-17475T=	ENSP00000426541.2:n.-18-17475T=
ENST00000505350.1:c.166-17475T=	ENSP00000481752.1:n.166-17475T=
ENST00000507379.5:c.166-28928T=	ENSP00000423224.1:n.166-28928T=
ENST00000509732.5:c.-18-17475T=	ENSP00000426541.1:n.-18-17475T=
NM_001127511.2:c.166-28928T=	NP_001120983.2:n.166-28928T=
NM_001354895.1:c.-18-17475T=	NP_001341824.1:n.-18-17475T=
NM_001354897.1:c.166-28928T=	NP_001341826.1:n.166-28928T=
NM_001354902.1:c.166-28928T=	NP_001341831.1:n.166-28928T=
NM_001127511.3:c.166-28928T=	NP_001120983.2:n.166-28928T=
NM_001354895.2:c.-18-17475T=	NP_001341824.1:n.-18-17475T=
NM_001354897.2:c.166-28928T=	NP_001341826.1:n.166-28928T=
NM_001354902.2:c.166-28928T=	NP_001341831.1:n.166-28928T=