Canonical Allele Identifier: CA658796609

Gene: APC

Linked Data

• ClinVar Variation Id: 537580
• ClinVar RCV Id: RCV003538535
• dbSNP Id: rs1311747020
• MyVariant Identifiers: chr5:g.112043280C>G (hg19) ; chr5:g.112707583C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707583C>G , CM000667.2:g.112707583C>G	GRCh38
NC_000005.9:g.112043280C>G , CM000667.1:g.112043280C>G	GRCh37
NC_000005.8:g.112071179C>G	NCBI36
NG_008481.4:g.20063C>G , LRG_130:g.20063C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.-135C>G	ENSP00000481752.1:n.-135C>G
ENST00000507379.6:c.-135C>G	ENSP00000423224.2:n.-135C>G
ENST00000509732.6:c.-85C>G	ENSP00000426541.2:n.-85C>G
ENST00000505350.1:c.-135C>G	ENSP00000481752.1:n.-135C>G
ENST00000507379.5:c.-135C>G	ENSP00000423224.1:n.-135C>G
ENST00000509732.5:c.-85C>G	ENSP00000426541.1:n.-85C>G
NM_001127511.2:c.-135C>G	NP_001120983.2:n.-135C>G
NM_001354895.1:c.-318C>G	NP_001341824.1:n.-318C>G
NM_001354897.1:c.-135C>G	NP_001341826.1:n.-135C>G
NM_001354902.1:c.-135C>G	NP_001341831.1:n.-135C>G
NM_001127511.3:c.-135C>G	NP_001120983.2:n.-135C>G
NM_001354895.2:c.-318C>G	NP_001341824.1:n.-318C>G
NM_001354897.2:c.-135C>G	NP_001341826.1:n.-135C>G
NM_001354902.2:c.-135C>G	NP_001341831.1:n.-135C>G