Canonical Allele Identifier: CA658796611

Gene: APC

Linked Data

• ClinVar Variation Id: 537649
• ClinVar RCV Id: RCV003538576
• dbSNP Id: rs79896135
• gnomAD v4: 5-112707585-C-A
• MyVariant Identifiers: chr5:g.112043282C>A (hg19) ; chr5:g.112707585C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707585C>A , CM000667.2:g.112707585C>A	GRCh38
NC_000005.9:g.112043282C>A , CM000667.1:g.112043282C>A	GRCh37
NC_000005.8:g.112071181C>A	NCBI36
NG_008481.4:g.20065C>A , LRG_130:g.20065C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.-133C>A	ENSP00000481752.1:n.-133C>A
ENST00000507379.6:c.-133C>A	ENSP00000423224.2:n.-133C>A
ENST00000509732.6:c.-83C>A	ENSP00000426541.2:n.-83C>A
ENST00000505350.1:c.-133C>A	ENSP00000481752.1:n.-133C>A
ENST00000507379.5:c.-133C>A	ENSP00000423224.1:n.-133C>A
ENST00000509732.5:c.-83C>A	ENSP00000426541.1:n.-83C>A
NM_001127511.2:c.-133C>A	NP_001120983.2:n.-133C>A
NM_001354895.1:c.-316C>A	NP_001341824.1:n.-316C>A
NM_001354897.1:c.-133C>A	NP_001341826.1:n.-133C>A
NM_001354902.1:c.-133C>A	NP_001341831.1:n.-133C>A
NM_001127511.3:c.-133C>A	NP_001120983.2:n.-133C>A
NM_001354895.2:c.-316C>A	NP_001341824.1:n.-316C>A
NM_001354897.2:c.-133C>A	NP_001341826.1:n.-133C>A
NM_001354902.2:c.-133C>A	NP_001341831.1:n.-133C>A