Canonical Allele Identifier: CA916079919

Gene: APC

Linked Data

• ClinVar Variation Id: 864178
• ClinVar RCV Id: RCV003650594
• dbSNP Id: rs1554086584

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840859_112840862delinsTGCG , CM000667.2:g.112840859_112840862delinsTGCG	GRCh38
NC_000005.9:g.112176556_112176559delinsTGCG , CM000667.1:g.112176556_112176559delinsTGCG	GRCh37
NC_000005.8:g.112204455_112204458delinsTGCG	NCBI36
NG_008481.4:g.153339_153342delinsTGCG , LRG_130:g.153339_153342delinsTGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5319_5322delinsTGCG	ENSP00000473355.2:p.Ser1774Ala
ENST00000505350.2:c.*5271_*5274delinsTGCG	ENSP00000481752.1:n.*5271_*5274delinsTGCG
ENST00000507379.6:c.5211_5214delinsTGCG	ENSP00000423224.2:p.Ser1738Ala
ENST00000509732.6:c.5265_5268delinsTGCG	ENSP00000426541.2:p.Ser1756Ala
ENST00000512211.7:c.5265_5268delinsTGCG	ENSP00000423828.3:p.Ser1756Ala
ENST00000257430.9:c.5265_5268delinsTGCG MANE Select	ENSP00000257430.4:p.Ser1756Ala
ENST00000257430.8:c.5265_5268delinsTGCG	ENSP00000257430.4:p.Ser1756Ala
ENST00000508376.6:c.5265_5268delinsTGCG	ENSP00000427089.2:p.Ser1756Ala
ENST00000508624.5:c.*4587_*4590delinsTGCG	ENSP00000424265.1:n.*4587_*4590delinsTGCG
ENST00000520401.1:c.230+11887_230+11890delinsTGCG
NM_000038.5:c.5265_5268delinsTGCG	NP_000029.2:p.Ser1756Ala
NM_001127510.2:c.5265_5268delinsTGCG	NP_001120982.1:p.Ser1756Ala
NM_001127511.2:c.5211_5214delinsTGCG	NP_001120983.2:p.Ser1738Ala
NM_001354895.1:c.5265_5268delinsTGCG	NP_001341824.1:p.Ser1756Ala
NM_001354896.1:c.5319_5322delinsTGCG	NP_001341825.1:p.Ser1774Ala
NM_001354897.1:c.5295_5298delinsTGCG	NP_001341826.1:p.Ser1766Ala
NM_001354898.1:c.5190_5193delinsTGCG	NP_001341827.1:p.Ser1731Ala
NM_001354899.1:c.5181_5184delinsTGCG	NP_001341828.1:p.Ser1728Ala
NM_001354900.1:c.5142_5145delinsTGCG	NP_001341829.1:p.Ser1715Ala
NM_001354901.1:c.5088_5091delinsTGCG	NP_001341830.1:p.Ser1697Ala
NM_001354902.1:c.4992_4995delinsTGCG	NP_001341831.1:p.Ser1665Ala
NM_001354903.1:c.4962_4965delinsTGCG	NP_001341832.1:p.Ser1655Ala
NM_001354904.1:c.4887_4890delinsTGCG	NP_001341833.1:p.Ser1630Ala
NM_001354905.1:c.4785_4788delinsTGCG	NP_001341834.1:p.Ser1596Ala
NM_001354906.1:c.4416_4419delinsTGCG	NP_001341835.1:p.Ser1473Ala
NM_000038.6:c.5265_5268delinsTGCG MANE Select	NP_000029.2:p.Ser1756Ala
NM_001127510.3:c.5265_5268delinsTGCG	NP_001120982.1:p.Ser1756Ala
NM_001127511.3:c.5211_5214delinsTGCG	NP_001120983.2:p.Ser1738Ala
NM_001354895.2:c.5265_5268delinsTGCG	NP_001341824.1:p.Ser1756Ala
NM_001354896.2:c.5319_5322delinsTGCG	NP_001341825.1:p.Ser1774Ala
NM_001354897.2:c.5295_5298delinsTGCG	NP_001341826.1:p.Ser1766Ala
NM_001354898.2:c.5190_5193delinsTGCG	NP_001341827.1:p.Ser1731Ala
NM_001354899.2:c.5181_5184delinsTGCG	NP_001341828.1:p.Ser1728Ala
NM_001354900.2:c.5142_5145delinsTGCG	NP_001341829.1:p.Ser1715Ala
NM_001354901.2:c.5088_5091delinsTGCG	NP_001341830.1:p.Ser1697Ala
NM_001354902.2:c.4992_4995delinsTGCG	NP_001341831.1:p.Ser1665Ala
NM_001354903.2:c.4962_4965delinsTGCG	NP_001341832.1:p.Ser1655Ala
NM_001354904.2:c.4887_4890delinsTGCG	NP_001341833.1:p.Ser1630Ala
NM_001354905.2:c.4785_4788delinsTGCG	NP_001341834.1:p.Ser1596Ala
NM_001354906.2:c.4416_4419delinsTGCG	NP_001341835.1:p.Ser1473Ala