Canonical Allele Identifier: CA16037855

Gene: APC

Linked Data

• ClinVar Variation Id: 855306
• ClinVar RCV Id: RCV003649362
• dbSNP Id: rs1561616981
• COSMIC: COSM6475536
• MyVariant Identifiers: chr5:g.112178897C>A (hg19) ; chr5:g.112843200C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843200C>A , CM000667.2:g.112843200C>A	GRCh38
NC_000005.9:g.112178897C>A , CM000667.1:g.112178897C>A	GRCh37
NC_000005.8:g.112206796C>A	NCBI36
NG_008481.4:g.155680C>A , LRG_130:g.155680C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7660C>A	ENSP00000473355.2:p.Pro2554Thr
ENST00000505350.2:c.*7612C>A	ENSP00000481752.1:n.*7612C>A
ENST00000507379.6:c.7552C>A	ENSP00000423224.2:p.Pro2518Thr
ENST00000509732.6:c.7606C>A	ENSP00000426541.2:p.Pro2536Thr
ENST00000512211.7:c.7606C>A	ENSP00000423828.3:p.Pro2536Thr
ENST00000257430.9:c.7606C>A MANE Select	ENSP00000257430.4:p.Pro2536Thr
ENST00000257430.8:c.7606C>A	ENSP00000257430.4:p.Pro2536Thr
ENST00000508376.6:c.7606C>A	ENSP00000427089.2:p.Pro2536Thr
ENST00000520401.1:c.231-13449C>A
NM_000038.5:c.7606C>A	NP_000029.2:p.Pro2536Thr
NM_001127510.2:c.7606C>A	NP_001120982.1:p.Pro2536Thr
NM_001127511.2:c.7552C>A	NP_001120983.2:p.Pro2518Thr
NM_001354895.1:c.7606C>A	NP_001341824.1:p.Pro2536Thr
NM_001354896.1:c.7660C>A	NP_001341825.1:p.Pro2554Thr
NM_001354897.1:c.7636C>A	NP_001341826.1:p.Pro2546Thr
NM_001354898.1:c.7531C>A	NP_001341827.1:p.Pro2511Thr
NM_001354899.1:c.7522C>A	NP_001341828.1:p.Pro2508Thr
NM_001354900.1:c.7483C>A	NP_001341829.1:p.Pro2495Thr
NM_001354901.1:c.7429C>A	NP_001341830.1:p.Pro2477Thr
NM_001354902.1:c.7333C>A	NP_001341831.1:p.Pro2445Thr
NM_001354903.1:c.7303C>A	NP_001341832.1:p.Pro2435Thr
NM_001354904.1:c.7228C>A	NP_001341833.1:p.Pro2410Thr
NM_001354905.1:c.7126C>A	NP_001341834.1:p.Pro2376Thr
NM_001354906.1:c.6757C>A	NP_001341835.1:p.Pro2253Thr
NM_000038.6:c.7606C>A MANE Select	NP_000029.2:p.Pro2536Thr
NM_001127510.3:c.7606C>A	NP_001120982.1:p.Pro2536Thr
NM_001127511.3:c.7552C>A	NP_001120983.2:p.Pro2518Thr
NM_001354895.2:c.7606C>A	NP_001341824.1:p.Pro2536Thr
NM_001354896.2:c.7660C>A	NP_001341825.1:p.Pro2554Thr
NM_001354897.2:c.7636C>A	NP_001341826.1:p.Pro2546Thr
NM_001354898.2:c.7531C>A	NP_001341827.1:p.Pro2511Thr
NM_001354899.2:c.7522C>A	NP_001341828.1:p.Pro2508Thr
NM_001354900.2:c.7483C>A	NP_001341829.1:p.Pro2495Thr
NM_001354901.2:c.7429C>A	NP_001341830.1:p.Pro2477Thr
NM_001354902.2:c.7333C>A	NP_001341831.1:p.Pro2445Thr
NM_001354903.2:c.7303C>A	NP_001341832.1:p.Pro2435Thr
NM_001354904.2:c.7228C>A	NP_001341833.1:p.Pro2410Thr
NM_001354905.2:c.7126C>A	NP_001341834.1:p.Pro2376Thr
NM_001354906.2:c.6757C>A	NP_001341835.1:p.Pro2253Thr