Canonical Allele Identifier: CA16038780

Gene: APC

Linked Data

• dbSNP Id: rs1263911481
• MyVariant Identifiers: chr5:g.112179326A>G (hg19) ; chr5:g.112843629A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843629A>G , CM000667.2:g.112843629A>G	GRCh38
NC_000005.9:g.112179326A>G , CM000667.1:g.112179326A>G	GRCh37
NC_000005.8:g.112207225A>G	NCBI36
NG_008481.4:g.156109A>G , LRG_130:g.156109A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8089A>G	ENSP00000473355.2:p.Thr2697Ala
ENST00000505350.2:c.*8041A>G	ENSP00000481752.1:n.*8041A>G
ENST00000507379.6:c.7981A>G	ENSP00000423224.2:p.Thr2661Ala
ENST00000509732.6:c.8035A>G	ENSP00000426541.2:p.Thr2679Ala
ENST00000512211.7:c.8035A>G	ENSP00000423828.3:p.Thr2679Ala
ENST00000257430.9:c.8035A>G MANE Select	ENSP00000257430.4:p.Thr2679Ala
ENST00000257430.8:c.8035A>G	ENSP00000257430.4:p.Thr2679Ala
ENST00000508376.6:c.8035A>G	ENSP00000427089.2:p.Thr2679Ala
ENST00000520401.1:c.231-13020A>G
NM_000038.5:c.8035A>G	NP_000029.2:p.Thr2679Ala
NM_001127510.2:c.8035A>G	NP_001120982.1:p.Thr2679Ala
NM_001127511.2:c.7981A>G	NP_001120983.2:p.Thr2661Ala
NM_001354895.1:c.8035A>G	NP_001341824.1:p.Thr2679Ala
NM_001354896.1:c.8089A>G	NP_001341825.1:p.Thr2697Ala
NM_001354897.1:c.8065A>G	NP_001341826.1:p.Thr2689Ala
NM_001354898.1:c.7960A>G	NP_001341827.1:p.Thr2654Ala
NM_001354899.1:c.7951A>G	NP_001341828.1:p.Thr2651Ala
NM_001354900.1:c.7912A>G	NP_001341829.1:p.Thr2638Ala
NM_001354901.1:c.7858A>G	NP_001341830.1:p.Thr2620Ala
NM_001354902.1:c.7762A>G	NP_001341831.1:p.Thr2588Ala
NM_001354903.1:c.7732A>G	NP_001341832.1:p.Thr2578Ala
NM_001354904.1:c.7657A>G	NP_001341833.1:p.Thr2553Ala
NM_001354905.1:c.7555A>G	NP_001341834.1:p.Thr2519Ala
NM_001354906.1:c.7186A>G	NP_001341835.1:p.Thr2396Ala
NM_000038.6:c.8035A>G MANE Select	NP_000029.2:p.Thr2679Ala
NM_001127510.3:c.8035A>G	NP_001120982.1:p.Thr2679Ala
NM_001127511.3:c.7981A>G	NP_001120983.2:p.Thr2661Ala
NM_001354895.2:c.8035A>G	NP_001341824.1:p.Thr2679Ala
NM_001354896.2:c.8089A>G	NP_001341825.1:p.Thr2697Ala
NM_001354897.2:c.8065A>G	NP_001341826.1:p.Thr2689Ala
NM_001354898.2:c.7960A>G	NP_001341827.1:p.Thr2654Ala
NM_001354899.2:c.7951A>G	NP_001341828.1:p.Thr2651Ala
NM_001354900.2:c.7912A>G	NP_001341829.1:p.Thr2638Ala
NM_001354901.2:c.7858A>G	NP_001341830.1:p.Thr2620Ala
NM_001354902.2:c.7762A>G	NP_001341831.1:p.Thr2588Ala
NM_001354903.2:c.7732A>G	NP_001341832.1:p.Thr2578Ala
NM_001354904.2:c.7657A>G	NP_001341833.1:p.Thr2553Ala
NM_001354905.2:c.7555A>G	NP_001341834.1:p.Thr2519Ala
NM_001354906.2:c.7186A>G	NP_001341835.1:p.Thr2396Ala