Canonical Allele Identifier: CA16032860

Gene: APC

Linked Data

• dbSNP Id: rs2149936334
• MyVariant Identifiers: chr5:g.112176566G>A (hg19) ; chr5:g.112840869G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112840869G>A , CM000667.2:g.112840869G>A	GRCh38
NC_000005.9:g.112176566G>A , CM000667.1:g.112176566G>A	GRCh37
NC_000005.8:g.112204465G>A	NCBI36
NG_008481.4:g.153349G>A , LRG_130:g.153349G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.5329G>A	ENSP00000473355.2:p.Ala1777Thr
ENST00000505350.2:c.*5281G>A	ENSP00000481752.1:n.*5281G>A
ENST00000507379.6:c.5221G>A	ENSP00000423224.2:p.Ala1741Thr
ENST00000509732.6:c.5275G>A	ENSP00000426541.2:p.Ala1759Thr
ENST00000512211.7:c.5275G>A	ENSP00000423828.3:p.Ala1759Thr
ENST00000257430.9:c.5275G>A MANE Select	ENSP00000257430.4:p.Ala1759Thr
ENST00000257430.8:c.5275G>A	ENSP00000257430.4:p.Ala1759Thr
ENST00000508376.6:c.5275G>A	ENSP00000427089.2:p.Ala1759Thr
ENST00000508624.5:c.*4597G>A	ENSP00000424265.1:n.*4597G>A
ENST00000520401.1:c.230+11897G>A
NM_000038.5:c.5275G>A	NP_000029.2:p.Ala1759Thr
NM_001127510.2:c.5275G>A	NP_001120982.1:p.Ala1759Thr
NM_001127511.2:c.5221G>A	NP_001120983.2:p.Ala1741Thr
NM_001354895.1:c.5275G>A	NP_001341824.1:p.Ala1759Thr
NM_001354896.1:c.5329G>A	NP_001341825.1:p.Ala1777Thr
NM_001354897.1:c.5305G>A	NP_001341826.1:p.Ala1769Thr
NM_001354898.1:c.5200G>A	NP_001341827.1:p.Ala1734Thr
NM_001354899.1:c.5191G>A	NP_001341828.1:p.Ala1731Thr
NM_001354900.1:c.5152G>A	NP_001341829.1:p.Ala1718Thr
NM_001354901.1:c.5098G>A	NP_001341830.1:p.Ala1700Thr
NM_001354902.1:c.5002G>A	NP_001341831.1:p.Ala1668Thr
NM_001354903.1:c.4972G>A	NP_001341832.1:p.Ala1658Thr
NM_001354904.1:c.4897G>A	NP_001341833.1:p.Ala1633Thr
NM_001354905.1:c.4795G>A	NP_001341834.1:p.Ala1599Thr
NM_001354906.1:c.4426G>A	NP_001341835.1:p.Ala1476Thr
NM_000038.6:c.5275G>A MANE Select	NP_000029.2:p.Ala1759Thr
NM_001127510.3:c.5275G>A	NP_001120982.1:p.Ala1759Thr
NM_001127511.3:c.5221G>A	NP_001120983.2:p.Ala1741Thr
NM_001354895.2:c.5275G>A	NP_001341824.1:p.Ala1759Thr
NM_001354896.2:c.5329G>A	NP_001341825.1:p.Ala1777Thr
NM_001354897.2:c.5305G>A	NP_001341826.1:p.Ala1769Thr
NM_001354898.2:c.5200G>A	NP_001341827.1:p.Ala1734Thr
NM_001354899.2:c.5191G>A	NP_001341828.1:p.Ala1731Thr
NM_001354900.2:c.5152G>A	NP_001341829.1:p.Ala1718Thr
NM_001354901.2:c.5098G>A	NP_001341830.1:p.Ala1700Thr
NM_001354902.2:c.5002G>A	NP_001341831.1:p.Ala1668Thr
NM_001354903.2:c.4972G>A	NP_001341832.1:p.Ala1658Thr
NM_001354904.2:c.4897G>A	NP_001341833.1:p.Ala1633Thr
NM_001354905.2:c.4795G>A	NP_001341834.1:p.Ala1599Thr
NM_001354906.2:c.4426G>A	NP_001341835.1:p.Ala1476Thr