Canonical Allele Identifier: CA2674863542

Gene: APC

Linked Data

• ClinVar Variation Id: 2797442
• ClinVar RCV Id: RCV003745863
• gnomAD v4: 5-112707584-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707584T>G , CM000667.2:g.112707584T>G	GRCh38
NC_000005.9:g.112043281T>G , CM000667.1:g.112043281T>G	GRCh37
NC_000005.8:g.112071180T>G	NCBI36
NG_008481.4:g.20064T>G , LRG_130:g.20064T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.-134T>G	ENSP00000481752.1:n.-134T>G
ENST00000507379.6:c.-134T>G	ENSP00000423224.2:n.-134T>G
ENST00000509732.6:c.-84T>G	ENSP00000426541.2:n.-84T>G
ENST00000505350.1:c.-134T>G	ENSP00000481752.1:n.-134T>G
ENST00000507379.5:c.-134T>G	ENSP00000423224.1:n.-134T>G
ENST00000509732.5:c.-84T>G	ENSP00000426541.1:n.-84T>G
NM_001127511.2:c.-134T>G	NP_001120983.2:n.-134T>G
NM_001354895.1:c.-317T>G	NP_001341824.1:n.-317T>G
NM_001354897.1:c.-134T>G	NP_001341826.1:n.-134T>G
NM_001354902.1:c.-134T>G	NP_001341831.1:n.-134T>G
NM_001127511.3:c.-134T>G	NP_001120983.2:n.-134T>G
NM_001354895.2:c.-317T>G	NP_001341824.1:n.-317T>G
NM_001354897.2:c.-134T>G	NP_001341826.1:n.-134T>G
NM_001354902.2:c.-134T>G	NP_001341831.1:n.-134T>G