Canonical Allele Identifier: CA1573442535

Gene: APC

Linked Data

• ClinVar Variation Id: 1001312
• ClinVar RCV Id: RCV003744794
• dbSNP Id: rs1750588164

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707609_112707610delinsTG , CM000667.2:g.112707609_112707610delinsTG	GRCh38
NC_000005.9:g.112043306_112043307delinsTG , CM000667.1:g.112043306_112043307delinsTG	GRCh37
NC_000005.8:g.112071205_112071206delinsTG	NCBI36
NG_008481.4:g.20089_20090delinsTG , LRG_130:g.20089_20090delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.-109_-108delinsTG	ENSP00000481752.1:n.-109_-108delinsTG
ENST00000507379.6:c.-109_-108delinsTG	ENSP00000423224.2:n.-109_-108delinsTG
ENST00000509732.6:c.-59_-58delinsTG	ENSP00000426541.2:n.-59_-58delinsTG
ENST00000505350.1:c.-109_-108delinsTG	ENSP00000481752.1:n.-109_-108delinsTG
ENST00000507379.5:c.-109_-108delinsTG	ENSP00000423224.1:n.-109_-108delinsTG
ENST00000509732.5:c.-59_-58delinsTG	ENSP00000426541.1:n.-59_-58delinsTG
NM_001127511.2:c.-109_-108delinsTG	NP_001120983.2:n.-109_-108delinsTG
NM_001354895.1:c.-292_-291delinsTG	NP_001341824.1:n.-292_-291delinsTG
NM_001354897.1:c.-109_-108delinsTG	NP_001341826.1:n.-109_-108delinsTG
NM_001354902.1:c.-109_-108delinsTG	NP_001341831.1:n.-109_-108delinsTG
NM_001127511.3:c.-109_-108delinsTG	NP_001120983.2:n.-109_-108delinsTG
NM_001354895.2:c.-292_-291delinsTG	NP_001341824.1:n.-292_-291delinsTG
NM_001354897.2:c.-109_-108delinsTG	NP_001341826.1:n.-109_-108delinsTG
NM_001354902.2:c.-109_-108delinsTG	NP_001341831.1:n.-109_-108delinsTG