Canonical Allele Identifier: CA2709768700

Gene: APC

Linked Data

• dbSNP Id: rs1580996349

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707603T>A , CM000667.2:g.112707603T>A	GRCh38
NC_000005.9:g.112043300T>A , CM000667.1:g.112043300T>A	GRCh37
NC_000005.8:g.112071199T>A	NCBI36
NG_008481.4:g.20083T>A , LRG_130:g.20083T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.-115T>A	ENSP00000481752.1:n.-115T>A
ENST00000507379.6:c.-115T>A	ENSP00000423224.2:n.-115T>A
ENST00000509732.6:c.-65T>A	ENSP00000426541.2:n.-65T>A
ENST00000505350.1:c.-115T>A	ENSP00000481752.1:n.-115T>A
ENST00000507379.5:c.-115T>A	ENSP00000423224.1:n.-115T>A
ENST00000509732.5:c.-65T>A	ENSP00000426541.1:n.-65T>A
NM_001127511.2:c.-115T>A	NP_001120983.2:n.-115T>A
NM_001354895.1:c.-298T>A	NP_001341824.1:n.-298T>A
NM_001354897.1:c.-115T>A	NP_001341826.1:n.-115T>A
NM_001354902.1:c.-115T>A	NP_001341831.1:n.-115T>A
NM_001127511.3:c.-115T>A	NP_001120983.2:n.-115T>A
NM_001354895.2:c.-298T>A	NP_001341824.1:n.-298T>A
NM_001354897.2:c.-115T>A	NP_001341826.1:n.-115T>A
NM_001354902.2:c.-115T>A	NP_001341831.1:n.-115T>A