Canonical Allele Identifier: CA023884

Gene: APC

Linked Data

• ClinVar Variation Id: 82326
• ClinVar RCV Id: RCV000073315
• dbSNP Id: rs77733015
• MyVariant Identifiers: chr5:g.112073396T>G (hg19) ; chr5:g.112737699T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112737699T>G , CM000667.2:g.112737699T>G	GRCh38
NC_000005.9:g.112073396T>G , CM000667.1:g.112073396T>G	GRCh37
NC_000005.8:g.112101295T>G	NCBI36
NG_008481.4:g.50179T>G , LRG_130:g.50179T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.166-17174T>G	ENSP00000481752.1:n.166-17174T>G
ENST00000507379.6:c.166-28627T>G	ENSP00000423224.2:n.166-28627T>G
ENST00000509732.6:c.-18-17174T>G	ENSP00000426541.2:n.-18-17174T>G
ENST00000505350.1:c.166-17174T>G	ENSP00000481752.1:n.166-17174T>G
ENST00000507379.5:c.166-28627T>G	ENSP00000423224.1:n.166-28627T>G
ENST00000509732.5:c.-18-17174T>G	ENSP00000426541.1:n.-18-17174T>G
NM_001127511.2:c.166-28627T>G	NP_001120983.2:n.166-28627T>G
NM_001354895.1:c.-18-17174T>G	NP_001341824.1:n.-18-17174T>G
NM_001354897.1:c.166-28627T>G	NP_001341826.1:n.166-28627T>G
NM_001354902.1:c.166-28627T>G	NP_001341831.1:n.166-28627T>G
NM_001127511.3:c.166-28627T>G	NP_001120983.2:n.166-28627T>G
NM_001354895.2:c.-18-17174T>G	NP_001341824.1:n.-18-17174T>G
NM_001354897.2:c.166-28627T>G	NP_001341826.1:n.166-28627T>G
NM_001354902.2:c.166-28627T>G	NP_001341831.1:n.166-28627T>G