Canonical Allele Identifier: CA1573458718

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112737805C= , CM000667.2:g.112737805C=	GRCh38
NC_000005.9:g.112073502C= , CM000667.1:g.112073502C=	GRCh37
NC_000005.8:g.112101401C=	NCBI36
NG_008481.4:g.50285C= , LRG_130:g.50285C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.166-17068C=	ENSP00000481752.1:n.166-17068C=
ENST00000507379.6:c.166-28521C=	ENSP00000423224.2:n.166-28521C=
ENST00000509732.6:c.-18-17068C=	ENSP00000426541.2:n.-18-17068C=
ENST00000505350.1:c.166-17068C=	ENSP00000481752.1:n.166-17068C=
ENST00000507379.5:c.166-28521C=	ENSP00000423224.1:n.166-28521C=
ENST00000509732.5:c.-18-17068C=	ENSP00000426541.1:n.-18-17068C=
NM_001127511.2:c.166-28521C=	NP_001120983.2:n.166-28521C=
NM_001354895.1:c.-18-17068C=	NP_001341824.1:n.-18-17068C=
NM_001354897.1:c.166-28521C=	NP_001341826.1:n.166-28521C=
NM_001354902.1:c.166-28521C=	NP_001341831.1:n.166-28521C=
NM_001127511.3:c.166-28521C=	NP_001120983.2:n.166-28521C=
NM_001354895.2:c.-18-17068C=	NP_001341824.1:n.-18-17068C=
NM_001354897.2:c.166-28521C=	NP_001341826.1:n.166-28521C=
NM_001354902.2:c.166-28521C=	NP_001341831.1:n.166-28521C=