Canonical Allele Identifier: CA1573458395

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112737562T= , CM000667.2:g.112737562T=	GRCh38
NC_000005.9:g.112073259T= , CM000667.1:g.112073259T=	GRCh37
NC_000005.8:g.112101158T=	NCBI36
NG_008481.4:g.50042T= , LRG_130:g.50042T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000505350.2:c.166-17311T=	ENSP00000481752.1:n.166-17311T=
ENST00000507379.6:c.166-28764T=	ENSP00000423224.2:n.166-28764T=
ENST00000509732.6:c.-18-17311T=	ENSP00000426541.2:n.-18-17311T=
ENST00000505350.1:c.166-17311T=	ENSP00000481752.1:n.166-17311T=
ENST00000507379.5:c.166-28764T=	ENSP00000423224.1:n.166-28764T=
ENST00000509732.5:c.-18-17311T=	ENSP00000426541.1:n.-18-17311T=
NM_001127511.2:c.166-28764T=	NP_001120983.2:n.166-28764T=
NM_001354895.1:c.-18-17311T=	NP_001341824.1:n.-18-17311T=
NM_001354897.1:c.166-28764T=	NP_001341826.1:n.166-28764T=
NM_001354902.1:c.166-28764T=	NP_001341831.1:n.166-28764T=
NM_001127511.3:c.166-28764T=	NP_001120983.2:n.166-28764T=
NM_001354895.2:c.-18-17311T=	NP_001341824.1:n.-18-17311T=
NM_001354897.2:c.166-28764T=	NP_001341826.1:n.166-28764T=
NM_001354902.2:c.166-28764T=	NP_001341831.1:n.166-28764T=