Canonical Allele Identifier: CA802028658

Gene: APC

Linked Data

• dbSNP Id: rs1318799223
• MyVariant Identifiers: chr5:g.112073252_112073256del (hg19) ; chr5:g.112737555_112737559del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112737555_112737559del , CM000667.2:g.112737555_112737559del	GRCh38
NC_000005.9:g.112073252_112073256del , CM000667.1:g.112073252_112073256del	GRCh37
NC_000005.8:g.112101151_112101155del	NCBI36
NG_008481.4:g.50035_50039del , LRG_130:g.50035_50039del

Transcript Alleles

HGVS	Amino-acid change
ENST00000505350.2:c.166-17318_166-17314del	ENSP00000481752.1:n.166-17318_166-17314de...
ENST00000507379.6:c.166-28771_166-28767del	ENSP00000423224.2:n.166-28771_166-28767de...
ENST00000509732.6:c.-18-17318_-18-17314del	ENSP00000426541.2:n.-18-17318_-18-17314de...
ENST00000505350.1:c.166-17318_166-17314del	ENSP00000481752.1:n.166-17318_166-17314de...
ENST00000507379.5:c.166-28771_166-28767del	ENSP00000423224.1:n.166-28771_166-28767de...
ENST00000509732.5:c.-18-17318_-18-17314del	ENSP00000426541.1:n.-18-17318_-18-17314de...
NM_001127511.2:c.166-28771_166-28767del	NP_001120983.2:n.166-28771_166-28767del
NM_001354895.1:c.-18-17318_-18-17314del	NP_001341824.1:n.-18-17318_-18-17314del
NM_001354897.1:c.166-28771_166-28767del	NP_001341826.1:n.166-28771_166-28767del
NM_001354902.1:c.166-28771_166-28767del	NP_001341831.1:n.166-28771_166-28767del
NM_001127511.3:c.166-28771_166-28767del	NP_001120983.2:n.166-28771_166-28767del
NM_001354895.2:c.-18-17318_-18-17314del	NP_001341824.1:n.-18-17318_-18-17314del
NM_001354897.2:c.166-28771_166-28767del	NP_001341826.1:n.166-28771_166-28767del
NM_001354902.2:c.166-28771_166-28767del	NP_001341831.1:n.166-28771_166-28767del