Canonical Allele Identifier: CA2578379433

Gene: APC

Linked Data

• gnomAD v4: 5-112707712-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707712C>A , CM000667.2:g.112707712C>A	GRCh38
NC_000005.9:g.112043409C>A , CM000667.1:g.112043409C>A	GRCh37
NC_000005.8:g.112071308C>A	NCBI36
NG_008481.4:g.20192C>A , LRG_130:g.20192C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.-6C>A	ENSP00000481752.1:n.-6C>A
ENST00000507379.6:c.-6C>A	ENSP00000423224.2:n.-6C>A
ENST00000509732.6:c.-19+63C>A	ENSP00000426541.2:n.-19+63C>A
ENST00000505350.1:c.-6C>A	ENSP00000481752.1:n.-6C>A
ENST00000507379.5:c.-6C>A	ENSP00000423224.1:n.-6C>A
ENST00000509732.5:c.-19+63C>A	ENSP00000426541.1:n.-19+63C>A
NM_001127511.2:c.-6C>A	NP_001120983.2:n.-6C>A
NM_001354895.1:c.-189C>A	NP_001341824.1:n.-189C>A
NM_001354897.1:c.-6C>A	NP_001341826.1:n.-6C>A
NM_001354902.1:c.-6C>A	NP_001341831.1:n.-6C>A
NM_001127511.3:c.-6C>A	NP_001120983.2:n.-6C>A
NM_001354895.2:c.-189C>A	NP_001341824.1:n.-189C>A
NM_001354897.2:c.-6C>A	NP_001341826.1:n.-6C>A
NM_001354902.2:c.-6C>A	NP_001341831.1:n.-6C>A