Canonical Allele Identifier: CA1573442737

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707803G= , CM000667.2:g.112707803G=	GRCh38
NC_000005.9:g.112043500G= , CM000667.1:g.112043500G=	GRCh37
NC_000005.8:g.112071399G=	NCBI36
NG_008481.4:g.20283G= , LRG_130:g.20283G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.86G=	ENSP00000481752.1:p.Gly29=
ENST00000507379.6:c.86G=	ENSP00000423224.2:p.Gly29=
ENST00000509732.6:c.-19+154G=	ENSP00000426541.2:n.-19+154G=
ENST00000505350.1:c.86G=	ENSP00000481752.1:p.Gly29=
ENST00000507379.5:c.86G=	ENSP00000423224.1:p.Gly29=
ENST00000509732.5:c.-19+154G=	ENSP00000426541.1:n.-19+154G=
NM_001127511.2:c.86G=	NP_001120983.2:p.Gly29=
NM_001354895.1:c.-98G=	NP_001341824.1:n.-98G=
NM_001354897.1:c.86G=	NP_001341826.1:p.Gly29=
NM_001354902.1:c.86G=	NP_001341831.1:p.Gly29=
NM_001127511.3:c.86G=	NP_001120983.2:p.Gly29=
NM_001354895.2:c.-98G=	NP_001341824.1:n.-98G=
NM_001354897.2:c.86G=	NP_001341826.1:p.Gly29=
NM_001354902.2:c.86G=	NP_001341831.1:p.Gly29=