Canonical Allele Identifier: CA124948535

Gene: APC

Linked Data

• dbSNP Id: rs746734486
• MyVariant Identifiers: chr5:g.112073145_112073149del (hg19) ; chr5:g.112737448_112737452del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112737453_112737457del , CM000667.2:g.112737453_112737457del	GRCh38
NC_000005.9:g.112073150_112073154del , CM000667.1:g.112073150_112073154del	GRCh37
NC_000005.8:g.112101049_112101053del	NCBI36
NG_008481.4:g.49933_49937del , LRG_130:g.49933_49937del

Transcript Alleles

HGVS	Amino-acid change
ENST00000505350.2:c.166-17420_166-17416del	ENSP00000481752.1:n.166-17420_166-17416de...
ENST00000507379.6:c.166-28873_166-28869del	ENSP00000423224.2:n.166-28873_166-28869de...
ENST00000509732.6:c.-18-17420_-18-17416del	ENSP00000426541.2:n.-18-17420_-18-17416de...
ENST00000505350.1:c.166-17420_166-17416del	ENSP00000481752.1:n.166-17420_166-17416de...
ENST00000507379.5:c.166-28873_166-28869del	ENSP00000423224.1:n.166-28873_166-28869de...
ENST00000509732.5:c.-18-17420_-18-17416del	ENSP00000426541.1:n.-18-17420_-18-17416de...
NM_001127511.2:c.166-28873_166-28869del	NP_001120983.2:n.166-28873_166-28869del
NM_001354895.1:c.-18-17420_-18-17416del	NP_001341824.1:n.-18-17420_-18-17416del
NM_001354897.1:c.166-28873_166-28869del	NP_001341826.1:n.166-28873_166-28869del
NM_001354902.1:c.166-28873_166-28869del	NP_001341831.1:n.166-28873_166-28869del
NM_001127511.3:c.166-28873_166-28869del	NP_001120983.2:n.166-28873_166-28869del
NM_001354895.2:c.-18-17420_-18-17416del	NP_001341824.1:n.-18-17420_-18-17416del
NM_001354897.2:c.166-28873_166-28869del	NP_001341826.1:n.166-28873_166-28869del
NM_001354902.2:c.166-28873_166-28869del	NP_001341831.1:n.166-28873_166-28869del