Canonical Allele Identifier: CA16028133

Gene: APC

Linked Data

• ClinVar Variation Id: 411437
• ClinVar RCV Id: RCV002230525
• dbSNP Id: rs1060503303
• MyVariant Identifiers: chr5:g.112174395A>C (hg19) ; chr5:g.112838698A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838698A>C , CM000667.2:g.112838698A>C	GRCh38
NC_000005.9:g.112174395A>C , CM000667.1:g.112174395A>C	GRCh37
NC_000005.8:g.112202294A>C	NCBI36
NG_008481.4:g.151178A>C , LRG_130:g.151178A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2769A>C	ENSP00000484935.2:n.2769A>C
ENST00000504915.3:c.3158A>C	ENSP00000473355.2:p.Gln1053Pro
ENST00000505350.2:c.*3110A>C	ENSP00000481752.1:n.*3110A>C
ENST00000507379.6:c.3050A>C	ENSP00000423224.2:p.Gln1017Pro
ENST00000509732.6:c.3104A>C	ENSP00000426541.2:p.Gln1035Pro
ENST00000512211.7:c.3104A>C	ENSP00000423828.3:p.Gln1035Pro
ENST00000257430.9:c.3104A>C MANE Select	ENSP00000257430.4:p.Gln1035Pro
ENST00000257430.8:c.3104A>C	ENSP00000257430.4:p.Gln1035Pro
ENST00000502371.2:c.1457A>C
ENST00000507379.5:c.3050A>C	ENSP00000423224.1:p.Gln1017Pro
ENST00000508376.6:c.3104A>C	ENSP00000427089.2:p.Gln1035Pro
ENST00000508624.5:c.*2426A>C	ENSP00000424265.1:n.*2426A>C
ENST00000512211.6:c.3104A>C	ENSP00000423828.2:p.Gln1035Pro
ENST00000520401.1:c.230+9726A>C
NM_000038.5:c.3104A>C	NP_000029.2:p.Gln1035Pro
NM_001127510.2:c.3104A>C	NP_001120982.1:p.Gln1035Pro
NM_001127511.2:c.3050A>C	NP_001120983.2:p.Gln1017Pro
NM_001354895.1:c.3104A>C	NP_001341824.1:p.Gln1035Pro
NM_001354896.1:c.3158A>C	NP_001341825.1:p.Gln1053Pro
NM_001354897.1:c.3134A>C	NP_001341826.1:p.Gln1045Pro
NM_001354898.1:c.3029A>C	NP_001341827.1:p.Gln1010Pro
NM_001354899.1:c.3020A>C	NP_001341828.1:p.Gln1007Pro
NM_001354900.1:c.2981A>C	NP_001341829.1:p.Gln994Pro
NM_001354901.1:c.2927A>C	NP_001341830.1:p.Gln976Pro
NM_001354902.1:c.2831A>C	NP_001341831.1:p.Gln944Pro
NM_001354903.1:c.2801A>C	NP_001341832.1:p.Gln934Pro
NM_001354904.1:c.2726A>C	NP_001341833.1:p.Gln909Pro
NM_001354905.1:c.2624A>C	NP_001341834.1:p.Gln875Pro
NM_001354906.1:c.2255A>C	NP_001341835.1:p.Gln752Pro
NM_000038.6:c.3104A>C MANE Select	NP_000029.2:p.Gln1035Pro
NM_001127510.3:c.3104A>C	NP_001120982.1:p.Gln1035Pro
NM_001127511.3:c.3050A>C	NP_001120983.2:p.Gln1017Pro
NM_001354895.2:c.3104A>C	NP_001341824.1:p.Gln1035Pro
NM_001354896.2:c.3158A>C	NP_001341825.1:p.Gln1053Pro
NM_001354897.2:c.3134A>C	NP_001341826.1:p.Gln1045Pro
NM_001354898.2:c.3029A>C	NP_001341827.1:p.Gln1010Pro
NM_001354899.2:c.3020A>C	NP_001341828.1:p.Gln1007Pro
NM_001354900.2:c.2981A>C	NP_001341829.1:p.Gln994Pro
NM_001354901.2:c.2927A>C	NP_001341830.1:p.Gln976Pro
NM_001354902.2:c.2831A>C	NP_001341831.1:p.Gln944Pro
NM_001354903.2:c.2801A>C	NP_001341832.1:p.Gln934Pro
NM_001354904.2:c.2726A>C	NP_001341833.1:p.Gln909Pro
NM_001354905.2:c.2624A>C	NP_001341834.1:p.Gln875Pro
NM_001354906.2:c.2255A>C	NP_001341835.1:p.Gln752Pro