Canonical Allele Identifier: CA16027964

Gene: APC

Linked Data

• ClinVar Variation Id: 934537
• ClinVar RCV Id: RCV003650661
• dbSNP Id: rs1765320980
• MyVariant Identifiers: chr5:g.112174323C>A (hg19) ; chr5:g.112838626C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838626C>A , CM000667.2:g.112838626C>A	GRCh38
NC_000005.9:g.112174323C>A , CM000667.1:g.112174323C>A	GRCh37
NC_000005.8:g.112202222C>A	NCBI36
NG_008481.4:g.151106C>A , LRG_130:g.151106C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2697C>A	ENSP00000484935.2:n.2697C>A
ENST00000504915.3:c.3086C>A	ENSP00000473355.2:p.Ala1029Glu
ENST00000505350.2:c.*3038C>A	ENSP00000481752.1:n.*3038C>A
ENST00000507379.6:c.2978C>A	ENSP00000423224.2:p.Ala993Glu
ENST00000509732.6:c.3032C>A	ENSP00000426541.2:p.Ala1011Glu
ENST00000512211.7:c.3032C>A	ENSP00000423828.3:p.Ala1011Glu
ENST00000257430.9:c.3032C>A MANE Select	ENSP00000257430.4:p.Ala1011Glu
ENST00000257430.8:c.3032C>A	ENSP00000257430.4:p.Ala1011Glu
ENST00000502371.2:c.1385C>A
ENST00000507379.5:c.2978C>A	ENSP00000423224.1:p.Ala993Glu
ENST00000508376.6:c.3032C>A	ENSP00000427089.2:p.Ala1011Glu
ENST00000508624.5:c.*2354C>A	ENSP00000424265.1:n.*2354C>A
ENST00000512211.6:c.3032C>A	ENSP00000423828.2:p.Ala1011Glu
ENST00000520401.1:c.230+9654C>A
NM_000038.5:c.3032C>A	NP_000029.2:p.Ala1011Glu
NM_001127510.2:c.3032C>A	NP_001120982.1:p.Ala1011Glu
NM_001127511.2:c.2978C>A	NP_001120983.2:p.Ala993Glu
NM_001354895.1:c.3032C>A	NP_001341824.1:p.Ala1011Glu
NM_001354896.1:c.3086C>A	NP_001341825.1:p.Ala1029Glu
NM_001354897.1:c.3062C>A	NP_001341826.1:p.Ala1021Glu
NM_001354898.1:c.2957C>A	NP_001341827.1:p.Ala986Glu
NM_001354899.1:c.2948C>A	NP_001341828.1:p.Ala983Glu
NM_001354900.1:c.2909C>A	NP_001341829.1:p.Ala970Glu
NM_001354901.1:c.2855C>A	NP_001341830.1:p.Ala952Glu
NM_001354902.1:c.2759C>A	NP_001341831.1:p.Ala920Glu
NM_001354903.1:c.2729C>A	NP_001341832.1:p.Ala910Glu
NM_001354904.1:c.2654C>A	NP_001341833.1:p.Ala885Glu
NM_001354905.1:c.2552C>A	NP_001341834.1:p.Ala851Glu
NM_001354906.1:c.2183C>A	NP_001341835.1:p.Ala728Glu
NM_000038.6:c.3032C>A MANE Select	NP_000029.2:p.Ala1011Glu
NM_001127510.3:c.3032C>A	NP_001120982.1:p.Ala1011Glu
NM_001127511.3:c.2978C>A	NP_001120983.2:p.Ala993Glu
NM_001354895.2:c.3032C>A	NP_001341824.1:p.Ala1011Glu
NM_001354896.2:c.3086C>A	NP_001341825.1:p.Ala1029Glu
NM_001354897.2:c.3062C>A	NP_001341826.1:p.Ala1021Glu
NM_001354898.2:c.2957C>A	NP_001341827.1:p.Ala986Glu
NM_001354899.2:c.2948C>A	NP_001341828.1:p.Ala983Glu
NM_001354900.2:c.2909C>A	NP_001341829.1:p.Ala970Glu
NM_001354901.2:c.2855C>A	NP_001341830.1:p.Ala952Glu
NM_001354902.2:c.2759C>A	NP_001341831.1:p.Ala920Glu
NM_001354903.2:c.2729C>A	NP_001341832.1:p.Ala910Glu
NM_001354904.2:c.2654C>A	NP_001341833.1:p.Ala885Glu
NM_001354905.2:c.2552C>A	NP_001341834.1:p.Ala851Glu
NM_001354906.2:c.2183C>A	NP_001341835.1:p.Ala728Glu