Canonical Allele Identifier: CA16023323

Gene: APC

Linked Data

• ClinVar Variation Id: 482405
• ClinVar RCV Id: RCV000573556 ; RCV003652012
• dbSNP Id: rs1554079213
• gnomAD v4: 5-112815579-C-T
• MyVariant Identifiers: chr5:g.112151276C>T (hg19) ; chr5:g.112815579C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112815579C>T , CM000667.2:g.112815579C>T	GRCh38
NC_000005.9:g.112151276C>T , CM000667.1:g.112151276C>T	GRCh37
NC_000005.8:g.112179175C>T	NCBI36
NG_008481.4:g.128059C>T , LRG_130:g.128059C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.919C>T	ENSP00000484935.2:p.His307Tyr
ENST00000504915.3:c.919C>T	ENSP00000473355.2:p.His307Tyr
ENST00000505084.2:n.975C>T
ENST00000505350.2:c.*925C>T	ENSP00000481752.1:n.*925C>T
ENST00000507379.6:c.865C>T	ENSP00000423224.2:p.His289Tyr
ENST00000509732.6:c.919C>T	ENSP00000426541.2:p.His307Tyr
ENST00000512211.7:c.919C>T	ENSP00000423828.3:p.His307Tyr
ENST00000257430.9:c.919C>T MANE Select	ENSP00000257430.4:p.His307Tyr
ENST00000257430.8:c.919C>T	ENSP00000257430.4:p.His307Tyr
ENST00000507379.5:c.865C>T	ENSP00000423224.1:p.His289Tyr
ENST00000508376.6:c.919C>T	ENSP00000427089.2:p.His307Tyr
ENST00000508624.5:c.*241C>T	ENSP00000424265.1:n.*241C>T
ENST00000512211.6:c.919C>T	ENSP00000423828.2:p.His307Tyr
NM_000038.5:c.919C>T	NP_000029.2:p.His307Tyr
NM_001127510.2:c.919C>T	NP_001120982.1:p.His307Tyr
NM_001127511.2:c.865C>T	NP_001120983.2:p.His289Tyr
NM_001354895.1:c.919C>T	NP_001341824.1:p.His307Tyr
NM_001354896.1:c.919C>T	NP_001341825.1:p.His307Tyr
NM_001354897.1:c.949C>T	NP_001341826.1:p.His317Tyr
NM_001354898.1:c.844C>T	NP_001341827.1:p.His282Tyr
NM_001354899.1:c.835C>T	NP_001341828.1:p.His279Tyr
NM_001354900.1:c.742C>T	NP_001341829.1:p.His248Tyr
NM_001354901.1:c.742C>T	NP_001341830.1:p.His248Tyr
NM_001354902.1:c.949C>T	NP_001341831.1:p.His317Tyr
NM_001354903.1:c.919C>T	NP_001341832.1:p.His307Tyr
NM_001354904.1:c.844C>T	NP_001341833.1:p.His282Tyr
NM_001354905.1:c.742C>T	NP_001341834.1:p.His248Tyr
NM_001354906.1:c.70C>T	NP_001341835.1:p.His24Tyr
NM_000038.6:c.919C>T MANE Select	NP_000029.2:p.His307Tyr
NM_001127510.3:c.919C>T	NP_001120982.1:p.His307Tyr
NM_001127511.3:c.865C>T	NP_001120983.2:p.His289Tyr
NM_001354895.2:c.919C>T	NP_001341824.1:p.His307Tyr
NM_001354896.2:c.919C>T	NP_001341825.1:p.His307Tyr
NM_001354897.2:c.949C>T	NP_001341826.1:p.His317Tyr
NM_001354898.2:c.844C>T	NP_001341827.1:p.His282Tyr
NM_001354899.2:c.835C>T	NP_001341828.1:p.His279Tyr
NM_001354900.2:c.742C>T	NP_001341829.1:p.His248Tyr
NM_001354901.2:c.742C>T	NP_001341830.1:p.His248Tyr
NM_001354902.2:c.949C>T	NP_001341831.1:p.His317Tyr
NM_001354903.2:c.919C>T	NP_001341832.1:p.His307Tyr
NM_001354904.2:c.844C>T	NP_001341833.1:p.His282Tyr
NM_001354905.2:c.742C>T	NP_001341834.1:p.His248Tyr
NM_001354906.2:c.70C>T	NP_001341835.1:p.His24Tyr