Canonical Allele Identifier: CA2825001374

Gene: APC

Linked Data

• ClinVar Variation Id: 3230589
• ClinVar RCV Id: RCV004520740

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840550del , CM000667.2:g.112840550del	GRCh38
NC_000005.9:g.112176247del , CM000667.1:g.112176247del	GRCh37
NC_000005.8:g.112204146del	NCBI36
NG_008481.4:g.153030del , LRG_130:g.153030del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5010del	ENSP00000473355.2:p.Thr1671GlnfsTer5
ENST00000505350.2:c.*4962del	ENSP00000481752.1:n.*4962del
ENST00000507379.6:c.4902del	ENSP00000423224.2:p.Thr1635GlnfsTer5
ENST00000509732.6:c.4956del	ENSP00000426541.2:p.Thr1653GlnfsTer5
ENST00000512211.7:c.4956del	ENSP00000423828.3:p.Thr1653GlnfsTer5
ENST00000257430.9:c.4956del MANE Select	ENSP00000257430.4:p.Thr1653GlnfsTer5
ENST00000257430.8:c.4956del	ENSP00000257430.4:p.Thr1653GlnfsTer5
ENST00000508376.6:c.4956del	ENSP00000427089.2:p.Thr1653GlnfsTer5
ENST00000508624.5:c.*4278del	ENSP00000424265.1:n.*4278del
ENST00000520401.1:c.230+11578del
NM_000038.5:c.4956del	NP_000029.2:p.Thr1653GlnfsTer5
NM_001127510.2:c.4956del	NP_001120982.1:p.Thr1653GlnfsTer5
NM_001127511.2:c.4902del	NP_001120983.2:p.Thr1635GlnfsTer5
NM_001354895.1:c.4956del	NP_001341824.1:p.Thr1653GlnfsTer5
NM_001354896.1:c.5010del	NP_001341825.1:p.Thr1671GlnfsTer5
NM_001354897.1:c.4986del	NP_001341826.1:p.Thr1663GlnfsTer5
NM_001354898.1:c.4881del	NP_001341827.1:p.Thr1628GlnfsTer5
NM_001354899.1:c.4872del	NP_001341828.1:p.Thr1625GlnfsTer5
NM_001354900.1:c.4833del	NP_001341829.1:p.Thr1612GlnfsTer5
NM_001354901.1:c.4779del	NP_001341830.1:p.Thr1594GlnfsTer5
NM_001354902.1:c.4683del	NP_001341831.1:p.Thr1562GlnfsTer5
NM_001354903.1:c.4653del	NP_001341832.1:p.Thr1552GlnfsTer5
NM_001354904.1:c.4578del	NP_001341833.1:p.Thr1527GlnfsTer5
NM_001354905.1:c.4476del	NP_001341834.1:p.Thr1493GlnfsTer5
NM_001354906.1:c.4107del	NP_001341835.1:p.Thr1370GlnfsTer5
NM_000038.6:c.4956del MANE Select	NP_000029.2:p.Thr1653GlnfsTer5
NM_001127510.3:c.4956del	NP_001120982.1:p.Thr1653GlnfsTer5
NM_001127511.3:c.4902del	NP_001120983.2:p.Thr1635GlnfsTer5
NM_001354895.2:c.4956del	NP_001341824.1:p.Thr1653GlnfsTer5
NM_001354896.2:c.5010del	NP_001341825.1:p.Thr1671GlnfsTer5
NM_001354897.2:c.4986del	NP_001341826.1:p.Thr1663GlnfsTer5
NM_001354898.2:c.4881del	NP_001341827.1:p.Thr1628GlnfsTer5
NM_001354899.2:c.4872del	NP_001341828.1:p.Thr1625GlnfsTer5
NM_001354900.2:c.4833del	NP_001341829.1:p.Thr1612GlnfsTer5
NM_001354901.2:c.4779del	NP_001341830.1:p.Thr1594GlnfsTer5
NM_001354902.2:c.4683del	NP_001341831.1:p.Thr1562GlnfsTer5
NM_001354903.2:c.4653del	NP_001341832.1:p.Thr1552GlnfsTer5
NM_001354904.2:c.4578del	NP_001341833.1:p.Thr1527GlnfsTer5
NM_001354905.2:c.4476del	NP_001341834.1:p.Thr1493GlnfsTer5
NM_001354906.2:c.4107del	NP_001341835.1:p.Thr1370GlnfsTer5