Canonical Allele Identifier: CA10582317

Gene: APC

Linked Data

• ClinVar Variation Id: 236605
• ClinVar RCV Id: RCV003535619
• dbSNP Id: rs878853449
• MyVariant Identifiers: chr5:g.112175992del (hg19) ; chr5:g.112840295del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840295del , CM000667.2:g.112840295del	GRCh38
NC_000005.9:g.112175992del , CM000667.1:g.112175992del	GRCh37
NC_000005.8:g.112203891del	NCBI36
NG_008481.4:g.152775del , LRG_130:g.152775del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.4755del	ENSP00000473355.2:p.Asp1586MetfsTer8
ENST00000505350.2:c.*4707del	ENSP00000481752.1:n.*4707del
ENST00000507379.6:c.4647del	ENSP00000423224.2:p.Asp1550MetfsTer8
ENST00000509732.6:c.4701del	ENSP00000426541.2:p.Asp1568MetfsTer8
ENST00000512211.7:c.4701del	ENSP00000423828.3:p.Asp1568MetfsTer8
ENST00000257430.9:c.4701del MANE Select	ENSP00000257430.4:p.Asp1568MetfsTer8
ENST00000257430.8:c.4701del	ENSP00000257430.4:p.Asp1568MetfsTer8
ENST00000508376.6:c.4701del	ENSP00000427089.2:p.Asp1568MetfsTer8
ENST00000508624.5:c.*4023del	ENSP00000424265.1:n.*4023del
ENST00000520401.1:c.230+11323del
NM_000038.5:c.4701del	NP_000029.2:p.Asp1568MetfsTer8
NM_001127510.2:c.4701del	NP_001120982.1:p.Asp1568MetfsTer8
NM_001127511.2:c.4647del	NP_001120983.2:p.Asp1550MetfsTer8
NM_001354895.1:c.4701del	NP_001341824.1:p.Asp1568MetfsTer8
NM_001354896.1:c.4755del	NP_001341825.1:p.Asp1586MetfsTer8
NM_001354897.1:c.4731del	NP_001341826.1:p.Asp1578MetfsTer8
NM_001354898.1:c.4626del	NP_001341827.1:p.Asp1543MetfsTer8
NM_001354899.1:c.4617del	NP_001341828.1:p.Asp1540MetfsTer8
NM_001354900.1:c.4578del	NP_001341829.1:p.Asp1527MetfsTer8
NM_001354901.1:c.4524del	NP_001341830.1:p.Asp1509MetfsTer8
NM_001354902.1:c.4428del	NP_001341831.1:p.Asp1477MetfsTer8
NM_001354903.1:c.4398del	NP_001341832.1:p.Asp1467MetfsTer8
NM_001354904.1:c.4323del	NP_001341833.1:p.Asp1442MetfsTer8
NM_001354905.1:c.4221del	NP_001341834.1:p.Asp1408MetfsTer8
NM_001354906.1:c.3852del	NP_001341835.1:p.Asp1285MetfsTer8
NM_000038.6:c.4701del MANE Select	NP_000029.2:p.Asp1568MetfsTer8
NM_001127510.3:c.4701del	NP_001120982.1:p.Asp1568MetfsTer8
NM_001127511.3:c.4647del	NP_001120983.2:p.Asp1550MetfsTer8
NM_001354895.2:c.4701del	NP_001341824.1:p.Asp1568MetfsTer8
NM_001354896.2:c.4755del	NP_001341825.1:p.Asp1586MetfsTer8
NM_001354897.2:c.4731del	NP_001341826.1:p.Asp1578MetfsTer8
NM_001354898.2:c.4626del	NP_001341827.1:p.Asp1543MetfsTer8
NM_001354899.2:c.4617del	NP_001341828.1:p.Asp1540MetfsTer8
NM_001354900.2:c.4578del	NP_001341829.1:p.Asp1527MetfsTer8
NM_001354901.2:c.4524del	NP_001341830.1:p.Asp1509MetfsTer8
NM_001354902.2:c.4428del	NP_001341831.1:p.Asp1477MetfsTer8
NM_001354903.2:c.4398del	NP_001341832.1:p.Asp1467MetfsTer8
NM_001354904.2:c.4323del	NP_001341833.1:p.Asp1442MetfsTer8
NM_001354905.2:c.4221del	NP_001341834.1:p.Asp1408MetfsTer8
NM_001354906.2:c.3852del	NP_001341835.1:p.Asp1285MetfsTer8