Canonical Allele Identifier: CA124948515

Gene: APC

Linked Data

• ClinVar Variation Id: 506405
• ClinVar RCV Id: RCV000600570
• dbSNP Id: rs116483942
• gnomAD v2: 5-112073101-G-A
• gnomAD v3: 5-112737404-G-A
• gnomAD v4: 5-112737404-G-A
• MyVariant Identifiers: chr5:g.112073101G>A (hg19) ; chr5:g.112737404G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112737404G>A , CM000667.2:g.112737404G>A	GRCh38
NC_000005.9:g.112073101G>A , CM000667.1:g.112073101G>A	GRCh37
NC_000005.8:g.112101000G>A	NCBI36
NG_008481.4:g.49884G>A , LRG_130:g.49884G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.166-17469G>A	ENSP00000481752.1:n.166-17469G>A
ENST00000507379.6:c.166-28922G>A	ENSP00000423224.2:n.166-28922G>A
ENST00000509732.6:c.-18-17469G>A	ENSP00000426541.2:n.-18-17469G>A
ENST00000505350.1:c.166-17469G>A	ENSP00000481752.1:n.166-17469G>A
ENST00000507379.5:c.166-28922G>A	ENSP00000423224.1:n.166-28922G>A
ENST00000509732.5:c.-18-17469G>A	ENSP00000426541.1:n.-18-17469G>A
NM_001127511.2:c.166-28922G>A	NP_001120983.2:n.166-28922G>A
NM_001354895.1:c.-18-17469G>A	NP_001341824.1:n.-18-17469G>A
NM_001354897.1:c.166-28922G>A	NP_001341826.1:n.166-28922G>A
NM_001354902.1:c.166-28922G>A	NP_001341831.1:n.166-28922G>A
NM_001127511.3:c.166-28922G>A	NP_001120983.2:n.166-28922G>A
NM_001354895.2:c.-18-17469G>A	NP_001341824.1:n.-18-17469G>A
NM_001354897.2:c.166-28922G>A	NP_001341826.1:n.166-28922G>A
NM_001354902.2:c.166-28922G>A	NP_001341831.1:n.166-28922G>A