Canonical Allele Identifier: CA1573442505

Gene: APC

Linked Data

• ClinVar Variation Id: 1003899
• ClinVar RCV Id: RCV002241754
• dbSNP Id: rs1750584693

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707592_112707593insT , CM000667.2:g.112707592_112707593insT	GRCh38
NC_000005.9:g.112043289_112043290insT , CM000667.1:g.112043289_112043290insT	GRCh37
NC_000005.8:g.112071188_112071189insT	NCBI36
NG_008481.4:g.20072_20073insT , LRG_130:g.20072_20073insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.-126_-125insT	ENSP00000481752.1:n.-126_-125insT
ENST00000507379.6:c.-126_-125insT	ENSP00000423224.2:n.-126_-125insT
ENST00000509732.6:c.-76_-75insT	ENSP00000426541.2:n.-76_-75insT
ENST00000505350.1:c.-126_-125insT	ENSP00000481752.1:n.-126_-125insT
ENST00000507379.5:c.-126_-125insT	ENSP00000423224.1:n.-126_-125insT
ENST00000509732.5:c.-76_-75insT	ENSP00000426541.1:n.-76_-75insT
NM_001127511.2:c.-126_-125insT	NP_001120983.2:n.-126_-125insT
NM_001354895.1:c.-309_-308insT	NP_001341824.1:n.-309_-308insT
NM_001354897.1:c.-126_-125insT	NP_001341826.1:n.-126_-125insT
NM_001354902.1:c.-126_-125insT	NP_001341831.1:n.-126_-125insT
NM_001127511.3:c.-126_-125insT	NP_001120983.2:n.-126_-125insT
NM_001354895.2:c.-309_-308insT	NP_001341824.1:n.-309_-308insT
NM_001354897.2:c.-126_-125insT	NP_001341826.1:n.-126_-125insT
NM_001354902.2:c.-126_-125insT	NP_001341831.1:n.-126_-125insT