Canonical Allele Identifier: CA16038376

Gene: APC

Linked Data

• ClinVar Variation Id: 1435937
• ClinVar RCV Id: RCV003772893
• dbSNP Id: rs2149994800
• MyVariant Identifiers: chr5:g.112179136A>G (hg19) ; chr5:g.112843439A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843439A>G , CM000667.2:g.112843439A>G	GRCh38
NC_000005.9:g.112179136A>G , CM000667.1:g.112179136A>G	GRCh37
NC_000005.8:g.112207035A>G	NCBI36
NG_008481.4:g.155919A>G , LRG_130:g.155919A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7899A>G	ENSP00000473355.2:p.Ile2633Met
ENST00000505350.2:c.*7851A>G	ENSP00000481752.1:n.*7851A>G
ENST00000507379.6:c.7791A>G	ENSP00000423224.2:p.Ile2597Met
ENST00000509732.6:c.7845A>G	ENSP00000426541.2:p.Ile2615Met
ENST00000512211.7:c.7845A>G	ENSP00000423828.3:p.Ile2615Met
ENST00000257430.9:c.7845A>G MANE Select	ENSP00000257430.4:p.Ile2615Met
ENST00000257430.8:c.7845A>G	ENSP00000257430.4:p.Ile2615Met
ENST00000508376.6:c.7845A>G	ENSP00000427089.2:p.Ile2615Met
ENST00000520401.1:c.231-13210A>G
NM_000038.5:c.7845A>G	NP_000029.2:p.Ile2615Met
NM_001127510.2:c.7845A>G	NP_001120982.1:p.Ile2615Met
NM_001127511.2:c.7791A>G	NP_001120983.2:p.Ile2597Met
NM_001354895.1:c.7845A>G	NP_001341824.1:p.Ile2615Met
NM_001354896.1:c.7899A>G	NP_001341825.1:p.Ile2633Met
NM_001354897.1:c.7875A>G	NP_001341826.1:p.Ile2625Met
NM_001354898.1:c.7770A>G	NP_001341827.1:p.Ile2590Met
NM_001354899.1:c.7761A>G	NP_001341828.1:p.Ile2587Met
NM_001354900.1:c.7722A>G	NP_001341829.1:p.Ile2574Met
NM_001354901.1:c.7668A>G	NP_001341830.1:p.Ile2556Met
NM_001354902.1:c.7572A>G	NP_001341831.1:p.Ile2524Met
NM_001354903.1:c.7542A>G	NP_001341832.1:p.Ile2514Met
NM_001354904.1:c.7467A>G	NP_001341833.1:p.Ile2489Met
NM_001354905.1:c.7365A>G	NP_001341834.1:p.Ile2455Met
NM_001354906.1:c.6996A>G	NP_001341835.1:p.Ile2332Met
NM_000038.6:c.7845A>G MANE Select	NP_000029.2:p.Ile2615Met
NM_001127510.3:c.7845A>G	NP_001120982.1:p.Ile2615Met
NM_001127511.3:c.7791A>G	NP_001120983.2:p.Ile2597Met
NM_001354895.2:c.7845A>G	NP_001341824.1:p.Ile2615Met
NM_001354896.2:c.7899A>G	NP_001341825.1:p.Ile2633Met
NM_001354897.2:c.7875A>G	NP_001341826.1:p.Ile2625Met
NM_001354898.2:c.7770A>G	NP_001341827.1:p.Ile2590Met
NM_001354899.2:c.7761A>G	NP_001341828.1:p.Ile2587Met
NM_001354900.2:c.7722A>G	NP_001341829.1:p.Ile2574Met
NM_001354901.2:c.7668A>G	NP_001341830.1:p.Ile2556Met
NM_001354902.2:c.7572A>G	NP_001341831.1:p.Ile2524Met
NM_001354903.2:c.7542A>G	NP_001341832.1:p.Ile2514Met
NM_001354904.2:c.7467A>G	NP_001341833.1:p.Ile2489Met
NM_001354905.2:c.7365A>G	NP_001341834.1:p.Ile2455Met
NM_001354906.2:c.6996A>G	NP_001341835.1:p.Ile2332Met