Canonical Allele Identifier: CA645372771

Gene: APC

Linked Data

• ClinVar Variation Id: 433617
• ClinVar RCV Id: RCV000502557 ; RCV003335413
• dbSNP Id: rs1554080070
• MyVariant Identifiers: chr5:g.112154942del (hg19) ; chr5:g.112819245del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112819245del , CM000667.2:g.112819245del	GRCh38
NC_000005.9:g.112154942del , CM000667.1:g.112154942del	GRCh37
NC_000005.8:g.112182841del	NCBI36
NG_008481.4:g.131725del , LRG_130:g.131725del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1213del	ENSP00000484935.2:p.Arg405GlufsTer?
ENST00000504915.3:c.1213del	ENSP00000473355.2:p.Arg405GlufsTer?
ENST00000505084.2:n.1269del
ENST00000505350.2:c.*1219del	ENSP00000481752.1:n.*1219del
ENST00000507379.6:c.1159del	ENSP00000423224.2:p.Arg387GlufsTer?
ENST00000509732.6:c.1213del	ENSP00000426541.2:p.Arg405GlufsTer?
ENST00000512211.7:c.1213del	ENSP00000423828.3:p.Arg405GlufsTer?
ENST00000257430.9:c.1213del MANE Select	ENSP00000257430.4:p.Arg405GlufsTer?
ENST00000257430.8:c.1213del	ENSP00000257430.4:p.Arg405GlufsTer?
ENST00000507379.5:c.1159del	ENSP00000423224.1:p.Arg387GlufsTer?
ENST00000508376.6:c.1213del	ENSP00000427089.2:p.Arg405GlufsTer?
ENST00000508624.5:c.*535del	ENSP00000424265.1:n.*535del
ENST00000512211.6:c.1213del	ENSP00000423828.2:p.Arg405GlufsTer?
NM_000038.5:c.1213del	NP_000029.2:p.Arg405GlufsTer?
NM_001127510.2:c.1213del	NP_001120982.1:p.Arg405GlufsTer?
NM_001127511.2:c.1159del	NP_001120983.2:p.Arg387GlufsTer?
NM_001354895.1:c.1213del	NP_001341824.1:p.Arg405GlufsTer?
NM_001354896.1:c.1213del	NP_001341825.1:p.Arg405GlufsTer?
NM_001354897.1:c.1243del	NP_001341826.1:p.Arg415GlufsTer?
NM_001354898.1:c.1138del	NP_001341827.1:p.Arg380GlufsTer?
NM_001354899.1:c.1129del	NP_001341828.1:p.Arg377GlufsTer?
NM_001354900.1:c.1036del	NP_001341829.1:p.Arg346GlufsTer?
NM_001354901.1:c.1036del	NP_001341830.1:p.Arg346GlufsTer?
NM_001354902.1:c.964-24del	NP_001341831.1:n.964-24del
NM_001354903.1:c.934-24del	NP_001341832.1:n.934-24del
NM_001354904.1:c.859-24del	NP_001341833.1:n.859-24del
NM_001354905.1:c.757-24del	NP_001341834.1:n.757-24del
NM_001354906.1:c.364del	NP_001341835.1:p.Arg122GlufsTer?
NM_000038.6:c.1213del MANE Select	NP_000029.2:p.Arg405GlufsTer?
NM_001127510.3:c.1213del	NP_001120982.1:p.Arg405GlufsTer?
NM_001127511.3:c.1159del	NP_001120983.2:p.Arg387GlufsTer?
NM_001354895.2:c.1213del	NP_001341824.1:p.Arg405GlufsTer?
NM_001354896.2:c.1213del	NP_001341825.1:p.Arg405GlufsTer?
NM_001354897.2:c.1243del	NP_001341826.1:p.Arg415GlufsTer?
NM_001354898.2:c.1138del	NP_001341827.1:p.Arg380GlufsTer?
NM_001354899.2:c.1129del	NP_001341828.1:p.Arg377GlufsTer?
NM_001354900.2:c.1036del	NP_001341829.1:p.Arg346GlufsTer?
NM_001354901.2:c.1036del	NP_001341830.1:p.Arg346GlufsTer?
NM_001354902.2:c.964-24del	NP_001341831.1:n.964-24del
NM_001354903.2:c.934-24del	NP_001341832.1:n.934-24del
NM_001354904.2:c.859-24del	NP_001341833.1:n.859-24del
NM_001354905.2:c.757-24del	NP_001341834.1:n.757-24del
NM_001354906.2:c.364del	NP_001341835.1:p.Arg122GlufsTer?