Canonical Allele Identifier: CA124924875

Gene: APC

Linked Data

• ClinVar Variation Id: 469850
• ClinVar RCV Id: RCV002231919
• dbSNP Id: rs1000470082
• gnomAD v3: 5-112707548-G-C
• gnomAD v4: 5-112707548-G-C
• MyVariant Identifiers: chr5:g.112043245G>C (hg19) ; chr5:g.112707548G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707548G>C , CM000667.2:g.112707548G>C	GRCh38
NC_000005.9:g.112043245G>C , CM000667.1:g.112043245G>C	GRCh37
NC_000005.8:g.112071144G>C	NCBI36
NG_008481.4:g.20028G>C , LRG_130:g.20028G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.-170G>C	ENSP00000481752.1:n.-170G>C
ENST00000507379.6:c.-170G>C	ENSP00000423224.2:n.-170G>C
ENST00000509732.6:c.-120G>C	ENSP00000426541.2:n.-120G>C
ENST00000505350.1:c.-170G>C	ENSP00000481752.1:n.-170G>C
ENST00000507379.5:c.-170G>C	ENSP00000423224.1:n.-170G>C
ENST00000509732.5:c.-120G>C	ENSP00000426541.1:n.-120G>C
NM_001127511.2:c.-170G>C	NP_001120983.2:n.-170G>C
NM_001354895.1:c.-353G>C	NP_001341824.1:n.-353G>C
NM_001354897.1:c.-170G>C	NP_001341826.1:n.-170G>C
NM_001354902.1:c.-170G>C	NP_001341831.1:n.-170G>C
NM_001127511.3:c.-170G>C	NP_001120983.2:n.-170G>C
NM_001354895.2:c.-353G>C	NP_001341824.1:n.-353G>C
NM_001354897.2:c.-170G>C	NP_001341826.1:n.-170G>C
NM_001354902.2:c.-170G>C	NP_001341831.1:n.-170G>C