Canonical Allele Identifier: CA16028162

Gene: APC

Linked Data

• ClinVar Variation Id: 923028
• ClinVar RCV Id: RCV001183414
• dbSNP Id: rs1765337280
• MyVariant Identifiers: chr5:g.112174407G>C (hg19) ; chr5:g.112838710G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838710G>C , CM000667.2:g.112838710G>C	GRCh38
NC_000005.9:g.112174407G>C , CM000667.1:g.112174407G>C	GRCh37
NC_000005.8:g.112202306G>C	NCBI36
NG_008481.4:g.151190G>C , LRG_130:g.151190G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2781G>C	ENSP00000484935.2:n.2781G>C
ENST00000504915.3:c.3170G>C	ENSP00000473355.2:p.Gly1057Ala
ENST00000505350.2:c.*3122G>C	ENSP00000481752.1:n.*3122G>C
ENST00000507379.6:c.3062G>C	ENSP00000423224.2:p.Gly1021Ala
ENST00000509732.6:c.3116G>C	ENSP00000426541.2:p.Gly1039Ala
ENST00000512211.7:c.3116G>C	ENSP00000423828.3:p.Gly1039Ala
ENST00000257430.9:c.3116G>C MANE Select	ENSP00000257430.4:p.Gly1039Ala
ENST00000257430.8:c.3116G>C	ENSP00000257430.4:p.Gly1039Ala
ENST00000502371.2:c.1469G>C
ENST00000507379.5:c.3062G>C	ENSP00000423224.1:p.Gly1021Ala
ENST00000508376.6:c.3116G>C	ENSP00000427089.2:p.Gly1039Ala
ENST00000508624.5:c.*2438G>C	ENSP00000424265.1:n.*2438G>C
ENST00000512211.6:c.3116G>C	ENSP00000423828.2:p.Gly1039Ala
ENST00000520401.1:c.230+9738G>C
NM_000038.5:c.3116G>C	NP_000029.2:p.Gly1039Ala
NM_001127510.2:c.3116G>C	NP_001120982.1:p.Gly1039Ala
NM_001127511.2:c.3062G>C	NP_001120983.2:p.Gly1021Ala
NM_001354895.1:c.3116G>C	NP_001341824.1:p.Gly1039Ala
NM_001354896.1:c.3170G>C	NP_001341825.1:p.Gly1057Ala
NM_001354897.1:c.3146G>C	NP_001341826.1:p.Gly1049Ala
NM_001354898.1:c.3041G>C	NP_001341827.1:p.Gly1014Ala
NM_001354899.1:c.3032G>C	NP_001341828.1:p.Gly1011Ala
NM_001354900.1:c.2993G>C	NP_001341829.1:p.Gly998Ala
NM_001354901.1:c.2939G>C	NP_001341830.1:p.Gly980Ala
NM_001354902.1:c.2843G>C	NP_001341831.1:p.Gly948Ala
NM_001354903.1:c.2813G>C	NP_001341832.1:p.Gly938Ala
NM_001354904.1:c.2738G>C	NP_001341833.1:p.Gly913Ala
NM_001354905.1:c.2636G>C	NP_001341834.1:p.Gly879Ala
NM_001354906.1:c.2267G>C	NP_001341835.1:p.Gly756Ala
NM_000038.6:c.3116G>C MANE Select	NP_000029.2:p.Gly1039Ala
NM_001127510.3:c.3116G>C	NP_001120982.1:p.Gly1039Ala
NM_001127511.3:c.3062G>C	NP_001120983.2:p.Gly1021Ala
NM_001354895.2:c.3116G>C	NP_001341824.1:p.Gly1039Ala
NM_001354896.2:c.3170G>C	NP_001341825.1:p.Gly1057Ala
NM_001354897.2:c.3146G>C	NP_001341826.1:p.Gly1049Ala
NM_001354898.2:c.3041G>C	NP_001341827.1:p.Gly1014Ala
NM_001354899.2:c.3032G>C	NP_001341828.1:p.Gly1011Ala
NM_001354900.2:c.2993G>C	NP_001341829.1:p.Gly998Ala
NM_001354901.2:c.2939G>C	NP_001341830.1:p.Gly980Ala
NM_001354902.2:c.2843G>C	NP_001341831.1:p.Gly948Ala
NM_001354903.2:c.2813G>C	NP_001341832.1:p.Gly938Ala
NM_001354904.2:c.2738G>C	NP_001341833.1:p.Gly913Ala
NM_001354905.2:c.2636G>C	NP_001341834.1:p.Gly879Ala
NM_001354906.2:c.2267G>C	NP_001341835.1:p.Gly756Ala