Canonical Allele Identifier: CA16037571

Gene: APC

Linked Data

• ClinVar Variation Id: 1759033
• ClinVar RCV Id: RCV002391439
• dbSNP Id: rs1554088378
• MyVariant Identifiers: chr5:g.112178756C>A (hg19) ; chr5:g.112843059C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843059C>A , CM000667.2:g.112843059C>A	GRCh38
NC_000005.9:g.112178756C>A , CM000667.1:g.112178756C>A	GRCh37
NC_000005.8:g.112206655C>A	NCBI36
NG_008481.4:g.155539C>A , LRG_130:g.155539C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7519C>A	ENSP00000473355.2:p.Pro2507Thr
ENST00000505350.2:c.*7471C>A	ENSP00000481752.1:n.*7471C>A
ENST00000507379.6:c.7411C>A	ENSP00000423224.2:p.Pro2471Thr
ENST00000509732.6:c.7465C>A	ENSP00000426541.2:p.Pro2489Thr
ENST00000512211.7:c.7465C>A	ENSP00000423828.3:p.Pro2489Thr
ENST00000257430.9:c.7465C>A MANE Select	ENSP00000257430.4:p.Pro2489Thr
ENST00000257430.8:c.7465C>A	ENSP00000257430.4:p.Pro2489Thr
ENST00000508376.6:c.7465C>A	ENSP00000427089.2:p.Pro2489Thr
ENST00000520401.1:c.231-13590C>A
NM_000038.5:c.7465C>A	NP_000029.2:p.Pro2489Thr
NM_001127510.2:c.7465C>A	NP_001120982.1:p.Pro2489Thr
NM_001127511.2:c.7411C>A	NP_001120983.2:p.Pro2471Thr
NM_001354895.1:c.7465C>A	NP_001341824.1:p.Pro2489Thr
NM_001354896.1:c.7519C>A	NP_001341825.1:p.Pro2507Thr
NM_001354897.1:c.7495C>A	NP_001341826.1:p.Pro2499Thr
NM_001354898.1:c.7390C>A	NP_001341827.1:p.Pro2464Thr
NM_001354899.1:c.7381C>A	NP_001341828.1:p.Pro2461Thr
NM_001354900.1:c.7342C>A	NP_001341829.1:p.Pro2448Thr
NM_001354901.1:c.7288C>A	NP_001341830.1:p.Pro2430Thr
NM_001354902.1:c.7192C>A	NP_001341831.1:p.Pro2398Thr
NM_001354903.1:c.7162C>A	NP_001341832.1:p.Pro2388Thr
NM_001354904.1:c.7087C>A	NP_001341833.1:p.Pro2363Thr
NM_001354905.1:c.6985C>A	NP_001341834.1:p.Pro2329Thr
NM_001354906.1:c.6616C>A	NP_001341835.1:p.Pro2206Thr
NM_000038.6:c.7465C>A MANE Select	NP_000029.2:p.Pro2489Thr
NM_001127510.3:c.7465C>A	NP_001120982.1:p.Pro2489Thr
NM_001127511.3:c.7411C>A	NP_001120983.2:p.Pro2471Thr
NM_001354895.2:c.7465C>A	NP_001341824.1:p.Pro2489Thr
NM_001354896.2:c.7519C>A	NP_001341825.1:p.Pro2507Thr
NM_001354897.2:c.7495C>A	NP_001341826.1:p.Pro2499Thr
NM_001354898.2:c.7390C>A	NP_001341827.1:p.Pro2464Thr
NM_001354899.2:c.7381C>A	NP_001341828.1:p.Pro2461Thr
NM_001354900.2:c.7342C>A	NP_001341829.1:p.Pro2448Thr
NM_001354901.2:c.7288C>A	NP_001341830.1:p.Pro2430Thr
NM_001354902.2:c.7192C>A	NP_001341831.1:p.Pro2398Thr
NM_001354903.2:c.7162C>A	NP_001341832.1:p.Pro2388Thr
NM_001354904.2:c.7087C>A	NP_001341833.1:p.Pro2363Thr
NM_001354905.2:c.6985C>A	NP_001341834.1:p.Pro2329Thr
NM_001354906.2:c.6616C>A	NP_001341835.1:p.Pro2206Thr