Canonical Allele Identifier: CA16038619

Gene: APC

Linked Data

• dbSNP Id: rs2149997013
• MyVariant Identifiers: chr5:g.112179252C>A (hg19) ; chr5:g.112843555C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843555C>A , CM000667.2:g.112843555C>A	GRCh38
NC_000005.9:g.112179252C>A , CM000667.1:g.112179252C>A	GRCh37
NC_000005.8:g.112207151C>A	NCBI36
NG_008481.4:g.156035C>A , LRG_130:g.156035C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8015C>A	ENSP00000473355.2:p.Thr2672Lys
ENST00000505350.2:c.*7967C>A	ENSP00000481752.1:n.*7967C>A
ENST00000507379.6:c.7907C>A	ENSP00000423224.2:p.Thr2636Lys
ENST00000509732.6:c.7961C>A	ENSP00000426541.2:p.Thr2654Lys
ENST00000512211.7:c.7961C>A	ENSP00000423828.3:p.Thr2654Lys
ENST00000257430.9:c.7961C>A MANE Select	ENSP00000257430.4:p.Thr2654Lys
ENST00000257430.8:c.7961C>A	ENSP00000257430.4:p.Thr2654Lys
ENST00000508376.6:c.7961C>A	ENSP00000427089.2:p.Thr2654Lys
ENST00000520401.1:c.231-13094C>A
NM_000038.5:c.7961C>A	NP_000029.2:p.Thr2654Lys
NM_001127510.2:c.7961C>A	NP_001120982.1:p.Thr2654Lys
NM_001127511.2:c.7907C>A	NP_001120983.2:p.Thr2636Lys
NM_001354895.1:c.7961C>A	NP_001341824.1:p.Thr2654Lys
NM_001354896.1:c.8015C>A	NP_001341825.1:p.Thr2672Lys
NM_001354897.1:c.7991C>A	NP_001341826.1:p.Thr2664Lys
NM_001354898.1:c.7886C>A	NP_001341827.1:p.Thr2629Lys
NM_001354899.1:c.7877C>A	NP_001341828.1:p.Thr2626Lys
NM_001354900.1:c.7838C>A	NP_001341829.1:p.Thr2613Lys
NM_001354901.1:c.7784C>A	NP_001341830.1:p.Thr2595Lys
NM_001354902.1:c.7688C>A	NP_001341831.1:p.Thr2563Lys
NM_001354903.1:c.7658C>A	NP_001341832.1:p.Thr2553Lys
NM_001354904.1:c.7583C>A	NP_001341833.1:p.Thr2528Lys
NM_001354905.1:c.7481C>A	NP_001341834.1:p.Thr2494Lys
NM_001354906.1:c.7112C>A	NP_001341835.1:p.Thr2371Lys
NM_000038.6:c.7961C>A MANE Select	NP_000029.2:p.Thr2654Lys
NM_001127510.3:c.7961C>A	NP_001120982.1:p.Thr2654Lys
NM_001127511.3:c.7907C>A	NP_001120983.2:p.Thr2636Lys
NM_001354895.2:c.7961C>A	NP_001341824.1:p.Thr2654Lys
NM_001354896.2:c.8015C>A	NP_001341825.1:p.Thr2672Lys
NM_001354897.2:c.7991C>A	NP_001341826.1:p.Thr2664Lys
NM_001354898.2:c.7886C>A	NP_001341827.1:p.Thr2629Lys
NM_001354899.2:c.7877C>A	NP_001341828.1:p.Thr2626Lys
NM_001354900.2:c.7838C>A	NP_001341829.1:p.Thr2613Lys
NM_001354901.2:c.7784C>A	NP_001341830.1:p.Thr2595Lys
NM_001354902.2:c.7688C>A	NP_001341831.1:p.Thr2563Lys
NM_001354903.2:c.7658C>A	NP_001341832.1:p.Thr2553Lys
NM_001354904.2:c.7583C>A	NP_001341833.1:p.Thr2528Lys
NM_001354905.2:c.7481C>A	NP_001341834.1:p.Thr2494Lys
NM_001354906.2:c.7112C>A	NP_001341835.1:p.Thr2371Lys