Canonical Allele Identifier: CA16038449

Gene: APC

Linked Data

• ClinVar Variation Id: 827303
• ClinVar RCV Id: RCV001026899 ; RCV003537435
• dbSNP Id: rs730881268
• gnomAD v4: 5-112843471-C-G
• MyVariant Identifiers: chr5:g.112179168C>G (hg19) ; chr5:g.112843471C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843471C>G , CM000667.2:g.112843471C>G	GRCh38
NC_000005.9:g.112179168C>G , CM000667.1:g.112179168C>G	GRCh37
NC_000005.8:g.112207067C>G	NCBI36
NG_008481.4:g.155951C>G , LRG_130:g.155951C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7931C>G	ENSP00000473355.2:p.Thr2644Ser
ENST00000505350.2:c.*7883C>G	ENSP00000481752.1:n.*7883C>G
ENST00000507379.6:c.7823C>G	ENSP00000423224.2:p.Thr2608Ser
ENST00000509732.6:c.7877C>G	ENSP00000426541.2:p.Thr2626Ser
ENST00000512211.7:c.7877C>G	ENSP00000423828.3:p.Thr2626Ser
ENST00000257430.9:c.7877C>G MANE Select	ENSP00000257430.4:p.Thr2626Ser
ENST00000257430.8:c.7877C>G	ENSP00000257430.4:p.Thr2626Ser
ENST00000508376.6:c.7877C>G	ENSP00000427089.2:p.Thr2626Ser
ENST00000520401.1:c.231-13178C>G
NM_000038.5:c.7877C>G	NP_000029.2:p.Thr2626Ser
NM_001127510.2:c.7877C>G	NP_001120982.1:p.Thr2626Ser
NM_001127511.2:c.7823C>G	NP_001120983.2:p.Thr2608Ser
NM_001354895.1:c.7877C>G	NP_001341824.1:p.Thr2626Ser
NM_001354896.1:c.7931C>G	NP_001341825.1:p.Thr2644Ser
NM_001354897.1:c.7907C>G	NP_001341826.1:p.Thr2636Ser
NM_001354898.1:c.7802C>G	NP_001341827.1:p.Thr2601Ser
NM_001354899.1:c.7793C>G	NP_001341828.1:p.Thr2598Ser
NM_001354900.1:c.7754C>G	NP_001341829.1:p.Thr2585Ser
NM_001354901.1:c.7700C>G	NP_001341830.1:p.Thr2567Ser
NM_001354902.1:c.7604C>G	NP_001341831.1:p.Thr2535Ser
NM_001354903.1:c.7574C>G	NP_001341832.1:p.Thr2525Ser
NM_001354904.1:c.7499C>G	NP_001341833.1:p.Thr2500Ser
NM_001354905.1:c.7397C>G	NP_001341834.1:p.Thr2466Ser
NM_001354906.1:c.7028C>G	NP_001341835.1:p.Thr2343Ser
NM_000038.6:c.7877C>G MANE Select	NP_000029.2:p.Thr2626Ser
NM_001127510.3:c.7877C>G	NP_001120982.1:p.Thr2626Ser
NM_001127511.3:c.7823C>G	NP_001120983.2:p.Thr2608Ser
NM_001354895.2:c.7877C>G	NP_001341824.1:p.Thr2626Ser
NM_001354896.2:c.7931C>G	NP_001341825.1:p.Thr2644Ser
NM_001354897.2:c.7907C>G	NP_001341826.1:p.Thr2636Ser
NM_001354898.2:c.7802C>G	NP_001341827.1:p.Thr2601Ser
NM_001354899.2:c.7793C>G	NP_001341828.1:p.Thr2598Ser
NM_001354900.2:c.7754C>G	NP_001341829.1:p.Thr2585Ser
NM_001354901.2:c.7700C>G	NP_001341830.1:p.Thr2567Ser
NM_001354902.2:c.7604C>G	NP_001341831.1:p.Thr2535Ser
NM_001354903.2:c.7574C>G	NP_001341832.1:p.Thr2525Ser
NM_001354904.2:c.7499C>G	NP_001341833.1:p.Thr2500Ser
NM_001354905.2:c.7397C>G	NP_001341834.1:p.Thr2466Ser
NM_001354906.2:c.7028C>G	NP_001341835.1:p.Thr2343Ser