Canonical Allele Identifier: CA1573453196

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112727778A= , CM000667.2:g.112727778A=	GRCh38
NC_000005.9:g.112063475A= , CM000667.1:g.112063475A=	GRCh37
NC_000005.8:g.112091374A=	NCBI36
NG_008481.4:g.40258A= , LRG_130:g.40258A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.165+19896A=	ENSP00000481752.1:n.165+19896A=
ENST00000507379.6:c.165+19896A=	ENSP00000423224.2:n.165+19896A=
ENST00000509732.6:c.-19+20129A=	ENSP00000426541.2:n.-19+20129A=
ENST00000505350.1:c.165+19896A=	ENSP00000481752.1:n.165+19896A=
ENST00000507379.5:c.165+19896A=	ENSP00000423224.1:n.165+19896A=
ENST00000509732.5:c.-19+20129A=	ENSP00000426541.1:n.-19+20129A=
NM_001127511.2:c.165+19896A=	NP_001120983.2:n.165+19896A=
NM_001354895.1:c.-19+19896A=	NP_001341824.1:n.-19+19896A=
NM_001354897.1:c.165+19896A=	NP_001341826.1:n.165+19896A=
NM_001354902.1:c.165+19896A=	NP_001341831.1:n.165+19896A=
NM_001127511.3:c.165+19896A=	NP_001120983.2:n.165+19896A=
NM_001354895.2:c.-19+19896A=	NP_001341824.1:n.-19+19896A=
NM_001354897.2:c.165+19896A=	NP_001341826.1:n.165+19896A=
NM_001354902.2:c.165+19896A=	NP_001341831.1:n.165+19896A=