Canonical Allele Identifier: CA802028642

Gene: APC

Linked Data

• dbSNP Id: rs1270749207
• MyVariant Identifiers: chr5:g.112073235_112073238del (hg19) ; chr5:g.112737538_112737541del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112737543_112737546del , CM000667.2:g.112737543_112737546del	GRCh38
NC_000005.9:g.112073240_112073243del , CM000667.1:g.112073240_112073243del	GRCh37
NC_000005.8:g.112101139_112101142del	NCBI36
NG_008481.4:g.50023_50026del , LRG_130:g.50023_50026del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.166-17330_166-17327del	ENSP00000481752.1:n.166-17330_166-17327del
ENST00000507379.6:c.166-28783_166-28780del	ENSP00000423224.2:n.166-28783_166-28780del
ENST00000509732.6:c.-18-17330_-18-17327del	ENSP00000426541.2:n.-18-17330_-18-17327del
ENST00000505350.1:c.166-17330_166-17327del	ENSP00000481752.1:n.166-17330_166-17327del
ENST00000507379.5:c.166-28783_166-28780del	ENSP00000423224.1:n.166-28783_166-28780del
ENST00000509732.5:c.-18-17330_-18-17327del	ENSP00000426541.1:n.-18-17330_-18-17327del
NM_001127511.2:c.166-28783_166-28780del	NP_001120983.2:n.166-28783_166-28780del
NM_001354895.1:c.-18-17330_-18-17327del	NP_001341824.1:n.-18-17330_-18-17327del
NM_001354897.1:c.166-28783_166-28780del	NP_001341826.1:n.166-28783_166-28780del
NM_001354902.1:c.166-28783_166-28780del	NP_001341831.1:n.166-28783_166-28780del
NM_001127511.3:c.166-28783_166-28780del	NP_001120983.2:n.166-28783_166-28780del
NM_001354895.2:c.-18-17330_-18-17327del	NP_001341824.1:n.-18-17330_-18-17327del
NM_001354897.2:c.166-28783_166-28780del	NP_001341826.1:n.166-28783_166-28780del
NM_001354902.2:c.166-28783_166-28780del	NP_001341831.1:n.166-28783_166-28780del