Canonical Allele Identifier: CA2674863493

Gene: APC

Linked Data

• gnomAD v4: 5-112707519-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707519C>A , CM000667.2:g.112707519C>A	GRCh38
NC_000005.9:g.112043216C>A , CM000667.1:g.112043216C>A	GRCh37
NC_000005.8:g.112071115C>A	NCBI36
NG_008481.4:g.19999C>A , LRG_130:g.19999C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509732.6:c.-149C>A	ENSP00000426541.2:n.-149C>A
ENST00000509732.5:c.-149C>A	ENSP00000426541.1:n.-149C>A
NM_001127511.2:c.-199C>A	NP_001120983.2:n.-199C>A
NM_001354895.1:c.-382C>A	NP_001341824.1:n.-382C>A
NM_001354897.1:c.-199C>A	NP_001341826.1:n.-199C>A
NM_001354902.1:c.-199C>A	NP_001341831.1:n.-199C>A
NM_001127511.3:c.-199C>A	NP_001120983.2:n.-199C>A
NM_001354895.2:c.-382C>A	NP_001341824.1:n.-382C>A
NM_001354897.2:c.-199C>A	NP_001341826.1:n.-199C>A
NM_001354902.2:c.-199C>A	NP_001341831.1:n.-199C>A