Canonical Allele Identifier: CA561893997

Gene: APC

Linked Data

• dbSNP Id: rs1488829183
• gnomAD v2: 5-112063585-A-C
• gnomAD v3: 5-112727888-A-C
• gnomAD v4: 5-112727888-A-C
• MyVariant Identifiers: chr5:g.112063585A>C (hg19) ; chr5:g.112727888A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112727888A>C , CM000667.2:g.112727888A>C	GRCh38
NC_000005.9:g.112063585A>C , CM000667.1:g.112063585A>C	GRCh37
NC_000005.8:g.112091484A>C	NCBI36
NG_008481.4:g.40368A>C , LRG_130:g.40368A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000505350.2:c.165+20006A>C	ENSP00000481752.1:n.165+20006A>C
ENST00000507379.6:c.165+20006A>C	ENSP00000423224.2:n.165+20006A>C
ENST00000509732.6:c.-19+20239A>C	ENSP00000426541.2:n.-19+20239A>C
ENST00000505350.1:c.165+20006A>C	ENSP00000481752.1:n.165+20006A>C
ENST00000507379.5:c.165+20006A>C	ENSP00000423224.1:n.165+20006A>C
ENST00000509732.5:c.-19+20239A>C	ENSP00000426541.1:n.-19+20239A>C
NM_001127511.2:c.165+20006A>C	NP_001120983.2:n.165+20006A>C
NM_001354895.1:c.-19+20006A>C	NP_001341824.1:n.-19+20006A>C
NM_001354897.1:c.165+20006A>C	NP_001341826.1:n.165+20006A>C
NM_001354902.1:c.165+20006A>C	NP_001341831.1:n.165+20006A>C
NM_001127511.3:c.165+20006A>C	NP_001120983.2:n.165+20006A>C
NM_001354895.2:c.-19+20006A>C	NP_001341824.1:n.-19+20006A>C
NM_001354897.2:c.165+20006A>C	NP_001341826.1:n.165+20006A>C
NM_001354902.2:c.165+20006A>C	NP_001341831.1:n.165+20006A>C