Canonical Allele Identifier: CA004112

Gene: APC

Linked Data

• ClinVar Variation Id: 188244
• ClinVar RCV Id: RCV000168200 ; RCV001850378 ; RCV002444673
• dbSNP Id: rs559510809
• MyVariant Identifiers: chr5:g.112154991G>A (hg19) ; chr5:g.112819294G>A (hg38)
• PubMed: PMID:20924072

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112819294G>A , CM000667.2:g.112819294G>A	GRCh38
NC_000005.9:g.112154991G>A , CM000667.1:g.112154991G>A	GRCh37
NC_000005.8:g.112182890G>A	NCBI36
NG_008481.4:g.131774G>A , LRG_130:g.131774G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.1262G>A	ENSP00000484935.2:p.Trp421Ter
ENST00000504915.3:c.1262G>A	ENSP00000473355.2:p.Trp421Ter
ENST00000505084.2:n.1318G>A
ENST00000505350.2:c.*1268G>A	ENSP00000481752.1:n.*1268G>A
ENST00000507379.6:c.1208G>A	ENSP00000423224.2:p.Trp403Ter
ENST00000509732.6:c.1262G>A	ENSP00000426541.2:p.Trp421Ter
ENST00000512211.7:c.1262G>A	ENSP00000423828.3:p.Trp421Ter
ENST00000257430.9:c.1262G>A MANE Select	ENSP00000257430.4:p.Trp421Ter
ENST00000257430.8:c.1262G>A	ENSP00000257430.4:p.Trp421Ter
ENST00000507379.5:c.1208G>A	ENSP00000423224.1:p.Trp403Ter
ENST00000508376.6:c.1262G>A	ENSP00000427089.2:p.Trp421Ter
ENST00000508624.5:c.*584G>A	ENSP00000424265.1:n.*584G>A
ENST00000512211.6:c.1262G>A	ENSP00000423828.2:p.Trp421Ter
NM_000038.5:c.1262G>A	NP_000029.2:p.Trp421Ter
NM_001127510.2:c.1262G>A	NP_001120982.1:p.Trp421Ter
NM_001127511.2:c.1208G>A	NP_001120983.2:p.Trp403Ter
NM_001354895.1:c.1262G>A	NP_001341824.1:p.Trp421Ter
NM_001354896.1:c.1262G>A	NP_001341825.1:p.Trp421Ter
NM_001354897.1:c.1292G>A	NP_001341826.1:p.Trp431Ter
NM_001354898.1:c.1187G>A	NP_001341827.1:p.Trp396Ter
NM_001354899.1:c.1178G>A	NP_001341828.1:p.Trp393Ter
NM_001354900.1:c.1085G>A	NP_001341829.1:p.Trp362Ter
NM_001354901.1:c.1085G>A	NP_001341830.1:p.Trp362Ter
NM_001354902.1:c.989G>A	NP_001341831.1:p.Trp330Ter
NM_001354903.1:c.959G>A	NP_001341832.1:p.Trp320Ter
NM_001354904.1:c.884G>A	NP_001341833.1:p.Trp295Ter
NM_001354905.1:c.782G>A	NP_001341834.1:p.Trp261Ter
NM_001354906.1:c.413G>A	NP_001341835.1:p.Trp138Ter
NM_000038.6:c.1262G>A MANE Select	NP_000029.2:p.Trp421Ter
NM_001127510.3:c.1262G>A	NP_001120982.1:p.Trp421Ter
NM_001127511.3:c.1208G>A	NP_001120983.2:p.Trp403Ter
NM_001354895.2:c.1262G>A	NP_001341824.1:p.Trp421Ter
NM_001354896.2:c.1262G>A	NP_001341825.1:p.Trp421Ter
NM_001354897.2:c.1292G>A	NP_001341826.1:p.Trp431Ter
NM_001354898.2:c.1187G>A	NP_001341827.1:p.Trp396Ter
NM_001354899.2:c.1178G>A	NP_001341828.1:p.Trp393Ter
NM_001354900.2:c.1085G>A	NP_001341829.1:p.Trp362Ter
NM_001354901.2:c.1085G>A	NP_001341830.1:p.Trp362Ter
NM_001354902.2:c.989G>A	NP_001341831.1:p.Trp330Ter
NM_001354903.2:c.959G>A	NP_001341832.1:p.Trp320Ter
NM_001354904.2:c.884G>A	NP_001341833.1:p.Trp295Ter
NM_001354905.2:c.782G>A	NP_001341834.1:p.Trp261Ter
NM_001354906.2:c.413G>A	NP_001341835.1:p.Trp138Ter