Canonical Allele Identifier: CA2674863491

Gene: APC

Linked Data

• gnomAD v4: 5-112707516-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707516C>T , CM000667.2:g.112707516C>T	GRCh38
NC_000005.9:g.112043213C>T , CM000667.1:g.112043213C>T	GRCh37
NC_000005.8:g.112071112C>T	NCBI36
NG_008481.4:g.19996C>T , LRG_130:g.19996C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509732.5:c.-152C>T	ENSP00000426541.1:n.-152C>T
NM_001127511.2:c.-202C>T	NP_001120983.2:n.-202C>T
NM_001354895.1:c.-385C>T	NP_001341824.1:n.-385C>T
NM_001354897.1:c.-202C>T	NP_001341826.1:n.-202C>T
NM_001354902.1:c.-202C>T	NP_001341831.1:n.-202C>T
NM_001127511.3:c.-202C>T	NP_001120983.2:n.-202C>T
NM_001354895.2:c.-385C>T	NP_001341824.1:n.-385C>T
NM_001354897.2:c.-202C>T	NP_001341826.1:n.-202C>T
NM_001354902.2:c.-202C>T	NP_001341831.1:n.-202C>T