Canonical Allele Identifier: CA248534

Gene: APC

Linked Data

• ClinVar Variation Id: 217957
• ClinVar RCV Id: RCV000202141 ; RCV000491545
• dbSNP Id: rs376213437
• MyVariant Identifiers: chr5:g.112102953T>G (hg19) ; chr5:g.112767256T>G (hg38)
• PubMed: PMID:20685668

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112767256T>G , CM000667.2:g.112767256T>G	GRCh38
NC_000005.9:g.112102953T>G , CM000667.1:g.112102953T>G	GRCh37
NC_000005.8:g.112130852T>G	NCBI36
NG_008481.4:g.79736T>G , LRG_130:g.79736T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.288T>G	ENSP00000484935.2:p.Tyr96Ter
ENST00000504915.3:c.288T>G	ENSP00000473355.2:p.Tyr96Ter
ENST00000505084.2:n.344T>G
ENST00000505350.2:c.*294T>G	ENSP00000481752.1:n.*294T>G
ENST00000507379.6:c.318T>G	ENSP00000423224.2:p.Tyr106Ter
ENST00000509732.6:c.288T>G	ENSP00000426541.2:p.Tyr96Ter
ENST00000512211.7:c.288T>G	ENSP00000423828.3:p.Tyr96Ter
ENST00000257430.9:c.288T>G MANE Select	ENSP00000257430.4:p.Tyr96Ter
ENST00000257430.8:c.288T>G	ENSP00000257430.4:p.Tyr96Ter
ENST00000507379.5:c.318T>G	ENSP00000423224.1:p.Tyr106Ter
ENST00000508376.6:c.288T>G	ENSP00000427089.2:p.Tyr96Ter
ENST00000508624.5:c.288T>G	ENSP00000424265.1:p.Tyr96Ter
ENST00000509732.5:c.288T>G	ENSP00000426541.1:p.Tyr96Ter
ENST00000512211.6:c.288T>G	ENSP00000423828.2:p.Tyr96Ter
NM_000038.5:c.288T>G	NP_000029.2:p.Tyr96Ter
NM_001127510.2:c.288T>G	NP_001120982.1:p.Tyr96Ter
NM_001127511.2:c.318T>G	NP_001120983.2:p.Tyr106Ter
NM_001354895.1:c.288T>G	NP_001341824.1:p.Tyr96Ter
NM_001354896.1:c.288T>G	NP_001341825.1:p.Tyr96Ter
NM_001354897.1:c.318T>G	NP_001341826.1:p.Tyr106Ter
NM_001354898.1:c.213T>G	NP_001341827.1:p.Tyr71Ter
NM_001354899.1:c.288T>G	NP_001341828.1:p.Tyr96Ter
NM_001354900.1:c.111T>G	NP_001341829.1:p.Tyr37Ter
NM_001354901.1:c.111T>G	NP_001341830.1:p.Tyr37Ter
NM_001354902.1:c.318T>G	NP_001341831.1:p.Tyr106Ter
NM_001354903.1:c.288T>G	NP_001341832.1:p.Tyr96Ter
NM_001354904.1:c.213T>G	NP_001341833.1:p.Tyr71Ter
NM_001354905.1:c.111T>G	NP_001341834.1:p.Tyr37Ter
NM_001354906.1:c.-748T>G	NP_001341835.1:n.-748T>G
NM_000038.6:c.288T>G MANE Select	NP_000029.2:p.Tyr96Ter
NM_001127510.3:c.288T>G	NP_001120982.1:p.Tyr96Ter
NM_001127511.3:c.318T>G	NP_001120983.2:p.Tyr106Ter
NM_001354895.2:c.288T>G	NP_001341824.1:p.Tyr96Ter
NM_001354896.2:c.288T>G	NP_001341825.1:p.Tyr96Ter
NM_001354897.2:c.318T>G	NP_001341826.1:p.Tyr106Ter
NM_001354898.2:c.213T>G	NP_001341827.1:p.Tyr71Ter
NM_001354899.2:c.288T>G	NP_001341828.1:p.Tyr96Ter
NM_001354900.2:c.111T>G	NP_001341829.1:p.Tyr37Ter
NM_001354901.2:c.111T>G	NP_001341830.1:p.Tyr37Ter
NM_001354902.2:c.318T>G	NP_001341831.1:p.Tyr106Ter
NM_001354903.2:c.288T>G	NP_001341832.1:p.Tyr96Ter
NM_001354904.2:c.213T>G	NP_001341833.1:p.Tyr71Ter
NM_001354905.2:c.111T>G	NP_001341834.1:p.Tyr37Ter
NM_001354906.2:c.-748T>G	NP_001341835.1:n.-748T>G