Canonical Allele Identifier: CA1573458788

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112737865G= , CM000667.2:g.112737865G=	GRCh38
NC_000005.9:g.112073562G= , CM000667.1:g.112073562G=	GRCh37
NC_000005.8:g.112101461G=	NCBI36
NG_008481.4:g.50345G= , LRG_130:g.50345G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.166-17008G=	ENSP00000481752.1:n.166-17008G=
ENST00000507379.6:c.166-28461G=	ENSP00000423224.2:n.166-28461G=
ENST00000509732.6:c.-18-17008G=	ENSP00000426541.2:n.-18-17008G=
ENST00000505350.1:c.166-17008G=	ENSP00000481752.1:n.166-17008G=
ENST00000507379.5:c.166-28461G=	ENSP00000423224.1:n.166-28461G=
ENST00000509732.5:c.-18-17008G=	ENSP00000426541.1:n.-18-17008G=
NM_000038.5:c.-79G=	NP_000029.2:n.-79G=
NM_001127510.2:c.-187G=	NP_001120982.1:n.-187G=
NM_001127511.2:c.166-28461G=	NP_001120983.2:n.166-28461G=
NM_001354895.1:c.-18-17008G=	NP_001341824.1:n.-18-17008G=
NM_001354896.1:c.-79G=	NP_001341825.1:n.-79G=
NM_001354897.1:c.166-28461G=	NP_001341826.1:n.166-28461G=
NM_001354898.1:c.-109G=	NP_001341827.1:n.-109G=
NM_001354899.1:c.-79G=	NP_001341828.1:n.-79G=
NM_001354900.1:c.-103G=	NP_001341829.1:n.-103G=
NM_001354901.1:c.-103G=	NP_001341830.1:n.-103G=
NM_001354902.1:c.166-28461G=	NP_001341831.1:n.166-28461G=
NM_001354903.1:c.-79G=	NP_001341832.1:n.-79G=
NM_001354904.1:c.-109G=	NP_001341833.1:n.-109G=
NM_001354905.1:c.-103G=	NP_001341834.1:n.-103G=
NM_001354906.1:c.-1114G=	NP_001341835.1:n.-1114G=
NM_001127511.3:c.166-28461G=	NP_001120983.2:n.166-28461G=
NM_001354895.2:c.-18-17008G=	NP_001341824.1:n.-18-17008G=
NM_001354897.2:c.166-28461G=	NP_001341826.1:n.166-28461G=
NM_001354902.2:c.166-28461G=	NP_001341831.1:n.166-28461G=