Canonical Allele Identifier: CA2573138781

Gene: APC

Linked Data

• ClinVar Variation Id: 1426422
• ClinVar RCV Id: RCV003772849
• dbSNP Id: rs2149629636

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707590_112707591delinsTT , CM000667.2:g.112707590_112707591delinsTT	GRCh38
NC_000005.9:g.112043287_112043288delinsTT , CM000667.1:g.112043287_112043288delinsTT	GRCh37
NC_000005.8:g.112071186_112071187delinsTT	NCBI36
NG_008481.4:g.20070_20071delinsTT , LRG_130:g.20070_20071delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.-128_-127delinsTT	ENSP00000481752.1:n.-128_-127delinsTT
ENST00000507379.6:c.-128_-127delinsTT	ENSP00000423224.2:n.-128_-127delinsTT
ENST00000509732.6:c.-78_-77delinsTT	ENSP00000426541.2:n.-78_-77delinsTT
ENST00000505350.1:c.-128_-127delinsTT	ENSP00000481752.1:n.-128_-127delinsTT
ENST00000507379.5:c.-128_-127delinsTT	ENSP00000423224.1:n.-128_-127delinsTT
ENST00000509732.5:c.-78_-77delinsTT	ENSP00000426541.1:n.-78_-77delinsTT
NM_001127511.2:c.-128_-127delinsTT	NP_001120983.2:n.-128_-127delinsTT
NM_001354895.1:c.-311_-310delinsTT	NP_001341824.1:n.-311_-310delinsTT
NM_001354897.1:c.-128_-127delinsTT	NP_001341826.1:n.-128_-127delinsTT
NM_001354902.1:c.-128_-127delinsTT	NP_001341831.1:n.-128_-127delinsTT
NM_001127511.3:c.-128_-127delinsTT	NP_001120983.2:n.-128_-127delinsTT
NM_001354895.2:c.-311_-310delinsTT	NP_001341824.1:n.-311_-310delinsTT
NM_001354897.2:c.-128_-127delinsTT	NP_001341826.1:n.-128_-127delinsTT
NM_001354902.2:c.-128_-127delinsTT	NP_001341831.1:n.-128_-127delinsTT