Canonical Allele Identifier: CA124941245

Gene: APC

Linked Data

• dbSNP Id: rs528740166
• gnomAD v2: 5-112063779-A-G
• gnomAD v3: 5-112728082-A-G
• gnomAD v4: 5-112728082-A-G
• MyVariant Identifiers: chr5:g.112063779A>G (hg19) ; chr5:g.112063779_112063781delinsGTT (hg19) ; chr5:g.112728082A>G (hg38) ; chr5:g.112728082_112728084delinsGTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112728082A>G , CM000667.2:g.112728082A>G	GRCh38
NC_000005.9:g.112063779A>G , CM000667.1:g.112063779A>G	GRCh37
NC_000005.8:g.112091678A>G	NCBI36
NG_008481.4:g.40562A>G , LRG_130:g.40562A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505350.2:c.165+20200A>G	ENSP00000481752.1:n.165+20200A>G
ENST00000507379.6:c.165+20200A>G	ENSP00000423224.2:n.165+20200A>G
ENST00000509732.6:c.-19+20433A>G	ENSP00000426541.2:n.-19+20433A>G
ENST00000505350.1:c.165+20200A>G	ENSP00000481752.1:n.165+20200A>G
ENST00000507379.5:c.165+20200A>G	ENSP00000423224.1:n.165+20200A>G
ENST00000509732.5:c.-19+20433A>G	ENSP00000426541.1:n.-19+20433A>G
NM_001127511.2:c.165+20200A>G	NP_001120983.2:n.165+20200A>G
NM_001354895.1:c.-19+20200A>G	NP_001341824.1:n.-19+20200A>G
NM_001354897.1:c.165+20200A>G	NP_001341826.1:n.165+20200A>G
NM_001354902.1:c.165+20200A>G	NP_001341831.1:n.165+20200A>G
NM_001127511.3:c.165+20200A>G	NP_001120983.2:n.165+20200A>G
NM_001354895.2:c.-19+20200A>G	NP_001341824.1:n.-19+20200A>G
NM_001354897.2:c.165+20200A>G	NP_001341826.1:n.165+20200A>G
NM_001354902.2:c.165+20200A>G	NP_001341831.1:n.165+20200A>G