Canonical Allele Identifier: CA2740094004

Gene: APC

Linked Data

• ClinVar Variation Id: 3001945
• ClinVar RCV Id: RCV003863008

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112839953_112839954delinsCG , CM000667.2:g.112839953_112839954delinsCG	GRCh38
NC_000005.9:g.112175650_112175651delinsCG , CM000667.1:g.112175650_112175651delinsCG	GRCh37
NC_000005.8:g.112203549_112203550delinsCG	NCBI36
NG_008481.4:g.152433_152434delinsCG , LRG_130:g.152433_152434delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4413_4414delinsCG	ENSP00000473355.2:p.Lys1472Glu
ENST00000505350.2:c.*4365_*4366delinsCG	ENSP00000481752.1:n.*4365_*4366delinsCG
ENST00000507379.6:c.4305_4306delinsCG	ENSP00000423224.2:p.Lys1436Glu
ENST00000509732.6:c.4359_4360delinsCG	ENSP00000426541.2:p.Lys1454Glu
ENST00000512211.7:c.4359_4360delinsCG	ENSP00000423828.3:p.Lys1454Glu
ENST00000257430.9:c.4359_4360delinsCG MANE Select	ENSP00000257430.4:p.Lys1454Glu
ENST00000257430.8:c.4359_4360delinsCG	ENSP00000257430.4:p.Lys1454Glu
ENST00000508376.6:c.4359_4360delinsCG	ENSP00000427089.2:p.Lys1454Glu
ENST00000508624.5:c.*3681_*3682delinsCG	ENSP00000424265.1:n.*3681_*3682delinsCG
ENST00000520401.1:c.230+10981_230+10982delinsCG
NM_000038.5:c.4359_4360delinsCG	NP_000029.2:p.Lys1454Glu
NM_001127510.2:c.4359_4360delinsCG	NP_001120982.1:p.Lys1454Glu
NM_001127511.2:c.4305_4306delinsCG	NP_001120983.2:p.Lys1436Glu
NM_001354895.1:c.4359_4360delinsCG	NP_001341824.1:p.Lys1454Glu
NM_001354896.1:c.4413_4414delinsCG	NP_001341825.1:p.Lys1472Glu
NM_001354897.1:c.4389_4390delinsCG	NP_001341826.1:p.Lys1464Glu
NM_001354898.1:c.4284_4285delinsCG	NP_001341827.1:p.Lys1429Glu
NM_001354899.1:c.4275_4276delinsCG	NP_001341828.1:p.Lys1426Glu
NM_001354900.1:c.4236_4237delinsCG	NP_001341829.1:p.Lys1413Glu
NM_001354901.1:c.4182_4183delinsCG	NP_001341830.1:p.Lys1395Glu
NM_001354902.1:c.4086_4087delinsCG	NP_001341831.1:p.Lys1363Glu
NM_001354903.1:c.4056_4057delinsCG	NP_001341832.1:p.Lys1353Glu
NM_001354904.1:c.3981_3982delinsCG	NP_001341833.1:p.Lys1328Glu
NM_001354905.1:c.3879_3880delinsCG	NP_001341834.1:p.Lys1294Glu
NM_001354906.1:c.3510_3511delinsCG	NP_001341835.1:p.Lys1171Glu
NM_000038.6:c.4359_4360delinsCG MANE Select	NP_000029.2:p.Lys1454Glu
NM_001127510.3:c.4359_4360delinsCG	NP_001120982.1:p.Lys1454Glu
NM_001127511.3:c.4305_4306delinsCG	NP_001120983.2:p.Lys1436Glu
NM_001354895.2:c.4359_4360delinsCG	NP_001341824.1:p.Lys1454Glu
NM_001354896.2:c.4413_4414delinsCG	NP_001341825.1:p.Lys1472Glu
NM_001354897.2:c.4389_4390delinsCG	NP_001341826.1:p.Lys1464Glu
NM_001354898.2:c.4284_4285delinsCG	NP_001341827.1:p.Lys1429Glu
NM_001354899.2:c.4275_4276delinsCG	NP_001341828.1:p.Lys1426Glu
NM_001354900.2:c.4236_4237delinsCG	NP_001341829.1:p.Lys1413Glu
NM_001354901.2:c.4182_4183delinsCG	NP_001341830.1:p.Lys1395Glu
NM_001354902.2:c.4086_4087delinsCG	NP_001341831.1:p.Lys1363Glu
NM_001354903.2:c.4056_4057delinsCG	NP_001341832.1:p.Lys1353Glu
NM_001354904.2:c.3981_3982delinsCG	NP_001341833.1:p.Lys1328Glu
NM_001354905.2:c.3879_3880delinsCG	NP_001341834.1:p.Lys1294Glu
NM_001354906.2:c.3510_3511delinsCG	NP_001341835.1:p.Lys1171Glu