Canonical Allele Identifier: CA16029904

Gene: APC

Linked Data

• ClinVar Variation Id: 2774985
• ClinVar RCV Id: RCV003585043
• dbSNP Id: rs2149901776
• MyVariant Identifiers: chr5:g.112175198C>G (hg19) ; chr5:g.112839501C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839501C>G , CM000667.2:g.112839501C>G	GRCh38
NC_000005.9:g.112175198C>G , CM000667.1:g.112175198C>G	GRCh37
NC_000005.8:g.112203097C>G	NCBI36
NG_008481.4:g.151981C>G , LRG_130:g.151981C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.3572C>G	ENSP00000484935.2:n.3572C>G
ENST00000504915.3:c.3961C>G	ENSP00000473355.2:p.Gln1321Glu
ENST00000505350.2:c.*3913C>G	ENSP00000481752.1:n.*3913C>G
ENST00000507379.6:c.3853C>G	ENSP00000423224.2:p.Gln1285Glu
ENST00000509732.6:c.3907C>G	ENSP00000426541.2:p.Gln1303Glu
ENST00000512211.7:c.3907C>G	ENSP00000423828.3:p.Gln1303Glu
ENST00000257430.9:c.3907C>G MANE Select	ENSP00000257430.4:p.Gln1303Glu
ENST00000257430.8:c.3907C>G	ENSP00000257430.4:p.Gln1303Glu
ENST00000502371.2:c.2260C>G
ENST00000508376.6:c.3907C>G	ENSP00000427089.2:p.Gln1303Glu
ENST00000508624.5:c.*3229C>G	ENSP00000424265.1:n.*3229C>G
ENST00000512211.6:c.3907C>G	ENSP00000423828.2:p.Gln1303Glu
ENST00000520401.1:c.230+10529C>G
NM_000038.5:c.3907C>G	NP_000029.2:p.Gln1303Glu
NM_001127510.2:c.3907C>G	NP_001120982.1:p.Gln1303Glu
NM_001127511.2:c.3853C>G	NP_001120983.2:p.Gln1285Glu
NM_001354895.1:c.3907C>G	NP_001341824.1:p.Gln1303Glu
NM_001354896.1:c.3961C>G	NP_001341825.1:p.Gln1321Glu
NM_001354897.1:c.3937C>G	NP_001341826.1:p.Gln1313Glu
NM_001354898.1:c.3832C>G	NP_001341827.1:p.Gln1278Glu
NM_001354899.1:c.3823C>G	NP_001341828.1:p.Gln1275Glu
NM_001354900.1:c.3784C>G	NP_001341829.1:p.Gln1262Glu
NM_001354901.1:c.3730C>G	NP_001341830.1:p.Gln1244Glu
NM_001354902.1:c.3634C>G	NP_001341831.1:p.Gln1212Glu
NM_001354903.1:c.3604C>G	NP_001341832.1:p.Gln1202Glu
NM_001354904.1:c.3529C>G	NP_001341833.1:p.Gln1177Glu
NM_001354905.1:c.3427C>G	NP_001341834.1:p.Gln1143Glu
NM_001354906.1:c.3058C>G	NP_001341835.1:p.Gln1020Glu
NM_000038.6:c.3907C>G MANE Select	NP_000029.2:p.Gln1303Glu
NM_001127510.3:c.3907C>G	NP_001120982.1:p.Gln1303Glu
NM_001127511.3:c.3853C>G	NP_001120983.2:p.Gln1285Glu
NM_001354895.2:c.3907C>G	NP_001341824.1:p.Gln1303Glu
NM_001354896.2:c.3961C>G	NP_001341825.1:p.Gln1321Glu
NM_001354897.2:c.3937C>G	NP_001341826.1:p.Gln1313Glu
NM_001354898.2:c.3832C>G	NP_001341827.1:p.Gln1278Glu
NM_001354899.2:c.3823C>G	NP_001341828.1:p.Gln1275Glu
NM_001354900.2:c.3784C>G	NP_001341829.1:p.Gln1262Glu
NM_001354901.2:c.3730C>G	NP_001341830.1:p.Gln1244Glu
NM_001354902.2:c.3634C>G	NP_001341831.1:p.Gln1212Glu
NM_001354903.2:c.3604C>G	NP_001341832.1:p.Gln1202Glu
NM_001354904.2:c.3529C>G	NP_001341833.1:p.Gln1177Glu
NM_001354905.2:c.3427C>G	NP_001341834.1:p.Gln1143Glu
NM_001354906.2:c.3058C>G	NP_001341835.1:p.Gln1020Glu