Canonical Allele Identifier: CA16028082

Gene: APC

Linked Data

• ClinVar Variation Id: 1727379
• ClinVar RCV Id: RCV002319894
• dbSNP Id: rs2149883939
• MyVariant Identifiers: chr5:g.112174373A>G (hg19) ; chr5:g.112838676A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838676A>G , CM000667.2:g.112838676A>G	GRCh38
NC_000005.9:g.112174373A>G , CM000667.1:g.112174373A>G	GRCh37
NC_000005.8:g.112202272A>G	NCBI36
NG_008481.4:g.151156A>G , LRG_130:g.151156A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2747A>G	ENSP00000484935.2:n.2747A>G
ENST00000504915.3:c.3136A>G	ENSP00000473355.2:p.Ser1046Gly
ENST00000505350.2:c.*3088A>G	ENSP00000481752.1:n.*3088A>G
ENST00000507379.6:c.3028A>G	ENSP00000423224.2:p.Ser1010Gly
ENST00000509732.6:c.3082A>G	ENSP00000426541.2:p.Ser1028Gly
ENST00000512211.7:c.3082A>G	ENSP00000423828.3:p.Ser1028Gly
ENST00000257430.9:c.3082A>G MANE Select	ENSP00000257430.4:p.Ser1028Gly
ENST00000257430.8:c.3082A>G	ENSP00000257430.4:p.Ser1028Gly
ENST00000502371.2:c.1435A>G
ENST00000507379.5:c.3028A>G	ENSP00000423224.1:p.Ser1010Gly
ENST00000508376.6:c.3082A>G	ENSP00000427089.2:p.Ser1028Gly
ENST00000508624.5:c.*2404A>G	ENSP00000424265.1:n.*2404A>G
ENST00000512211.6:c.3082A>G	ENSP00000423828.2:p.Ser1028Gly
ENST00000520401.1:c.230+9704A>G
NM_000038.5:c.3082A>G	NP_000029.2:p.Ser1028Gly
NM_001127510.2:c.3082A>G	NP_001120982.1:p.Ser1028Gly
NM_001127511.2:c.3028A>G	NP_001120983.2:p.Ser1010Gly
NM_001354895.1:c.3082A>G	NP_001341824.1:p.Ser1028Gly
NM_001354896.1:c.3136A>G	NP_001341825.1:p.Ser1046Gly
NM_001354897.1:c.3112A>G	NP_001341826.1:p.Ser1038Gly
NM_001354898.1:c.3007A>G	NP_001341827.1:p.Ser1003Gly
NM_001354899.1:c.2998A>G	NP_001341828.1:p.Ser1000Gly
NM_001354900.1:c.2959A>G	NP_001341829.1:p.Ser987Gly
NM_001354901.1:c.2905A>G	NP_001341830.1:p.Ser969Gly
NM_001354902.1:c.2809A>G	NP_001341831.1:p.Ser937Gly
NM_001354903.1:c.2779A>G	NP_001341832.1:p.Ser927Gly
NM_001354904.1:c.2704A>G	NP_001341833.1:p.Ser902Gly
NM_001354905.1:c.2602A>G	NP_001341834.1:p.Ser868Gly
NM_001354906.1:c.2233A>G	NP_001341835.1:p.Ser745Gly
NM_000038.6:c.3082A>G MANE Select	NP_000029.2:p.Ser1028Gly
NM_001127510.3:c.3082A>G	NP_001120982.1:p.Ser1028Gly
NM_001127511.3:c.3028A>G	NP_001120983.2:p.Ser1010Gly
NM_001354895.2:c.3082A>G	NP_001341824.1:p.Ser1028Gly
NM_001354896.2:c.3136A>G	NP_001341825.1:p.Ser1046Gly
NM_001354897.2:c.3112A>G	NP_001341826.1:p.Ser1038Gly
NM_001354898.2:c.3007A>G	NP_001341827.1:p.Ser1003Gly
NM_001354899.2:c.2998A>G	NP_001341828.1:p.Ser1000Gly
NM_001354900.2:c.2959A>G	NP_001341829.1:p.Ser987Gly
NM_001354901.2:c.2905A>G	NP_001341830.1:p.Ser969Gly
NM_001354902.2:c.2809A>G	NP_001341831.1:p.Ser937Gly
NM_001354903.2:c.2779A>G	NP_001341832.1:p.Ser927Gly
NM_001354904.2:c.2704A>G	NP_001341833.1:p.Ser902Gly
NM_001354905.2:c.2602A>G	NP_001341834.1:p.Ser868Gly
NM_001354906.2:c.2233A>G	NP_001341835.1:p.Ser745Gly