Canonical Allele Identifier: CA2739274986

Gene: APC

Linked Data

• ClinVar Variation Id: 2819217
• ClinVar RCV Id: RCV003650884

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707821_112707822delinsTT , CM000667.2:g.112707821_112707822delinsTT	GRCh38
NC_000005.9:g.112043518_112043519delinsTT , CM000667.1:g.112043518_112043519delinsTT	GRCh37
NC_000005.8:g.112071417_112071418delinsTT	NCBI36
NG_008481.4:g.20301_20302delinsTT , LRG_130:g.20301_20302delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.104_105delinsTT	ENSP00000481752.1:p.Arg35Leu
ENST00000507379.6:c.104_105delinsTT	ENSP00000423224.2:p.Arg35Leu
ENST00000509732.6:c.-19+172_-19+173delinsTT	ENSP00000426541.2:n.-19+172_-19+173delinsTT
ENST00000505350.1:c.104_105delinsTT	ENSP00000481752.1:p.Arg35Leu
ENST00000507379.5:c.104_105delinsTT	ENSP00000423224.1:p.Arg35Leu
ENST00000509732.5:c.-19+172_-19+173delinsTT	ENSP00000426541.1:n.-19+172_-19+173delinsTT
NM_001127511.2:c.104_105delinsTT	NP_001120983.2:p.Arg35Leu
NM_001354895.1:c.-80_-79delinsTT	NP_001341824.1:n.-80_-79delinsTT
NM_001354897.1:c.104_105delinsTT	NP_001341826.1:p.Arg35Leu
NM_001354902.1:c.104_105delinsTT	NP_001341831.1:p.Arg35Leu
NM_001127511.3:c.104_105delinsTT	NP_001120983.2:p.Arg35Leu
NM_001354895.2:c.-80_-79delinsTT	NP_001341824.1:n.-80_-79delinsTT
NM_001354897.2:c.104_105delinsTT	NP_001341826.1:p.Arg35Leu
NM_001354902.2:c.104_105delinsTT	NP_001341831.1:p.Arg35Leu