Canonical Allele Identifier: CA1573458785

Gene: APC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112737862T= , CM000667.2:g.112737862T=	GRCh38
NC_000005.9:g.112073559T= , CM000667.1:g.112073559T=	GRCh37
NC_000005.8:g.112101458T=	NCBI36
NG_008481.4:g.50342T= , LRG_130:g.50342T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.166-17011T=	ENSP00000481752.1:n.166-17011T=
ENST00000507379.6:c.166-28464T=	ENSP00000423224.2:n.166-28464T=
ENST00000509732.6:c.-18-17011T=	ENSP00000426541.2:n.-18-17011T=
ENST00000505350.1:c.166-17011T=	ENSP00000481752.1:n.166-17011T=
ENST00000507379.5:c.166-28464T=	ENSP00000423224.1:n.166-28464T=
ENST00000509732.5:c.-18-17011T=	ENSP00000426541.1:n.-18-17011T=
NM_000038.5:c.-82T=	NP_000029.2:n.-82T=
NM_001127510.2:c.-190T=	NP_001120982.1:n.-190T=
NM_001127511.2:c.166-28464T=	NP_001120983.2:n.166-28464T=
NM_001354895.1:c.-18-17011T=	NP_001341824.1:n.-18-17011T=
NM_001354896.1:c.-82T=	NP_001341825.1:n.-82T=
NM_001354897.1:c.166-28464T=	NP_001341826.1:n.166-28464T=
NM_001354898.1:c.-112T=	NP_001341827.1:n.-112T=
NM_001354899.1:c.-82T=	NP_001341828.1:n.-82T=
NM_001354900.1:c.-106T=	NP_001341829.1:n.-106T=
NM_001354901.1:c.-106T=	NP_001341830.1:n.-106T=
NM_001354902.1:c.166-28464T=	NP_001341831.1:n.166-28464T=
NM_001354903.1:c.-82T=	NP_001341832.1:n.-82T=
NM_001354904.1:c.-112T=	NP_001341833.1:n.-112T=
NM_001354905.1:c.-106T=	NP_001341834.1:n.-106T=
NM_001354906.1:c.-1117T=	NP_001341835.1:n.-1117T=
NM_001127511.3:c.166-28464T=	NP_001120983.2:n.166-28464T=
NM_001354895.2:c.-18-17011T=	NP_001341824.1:n.-18-17011T=
NM_001354897.2:c.166-28464T=	NP_001341826.1:n.166-28464T=
NM_001354902.2:c.166-28464T=	NP_001341831.1:n.166-28464T=