Canonical Allele Identifier: CA16038715

Gene: APC

Linked Data

• dbSNP Id: rs2149997725
• gnomAD v4: 5-112843596-A-G
• MyVariant Identifiers: chr5:g.112179293A>G (hg19) ; chr5:g.112843596A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843596A>G , CM000667.2:g.112843596A>G	GRCh38
NC_000005.9:g.112179293A>G , CM000667.1:g.112179293A>G	GRCh37
NC_000005.8:g.112207192A>G	NCBI36
NG_008481.4:g.156076A>G , LRG_130:g.156076A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8056A>G	ENSP00000473355.2:p.Asn2686Asp
ENST00000505350.2:c.*8008A>G	ENSP00000481752.1:n.*8008A>G
ENST00000507379.6:c.7948A>G	ENSP00000423224.2:p.Asn2650Asp
ENST00000509732.6:c.8002A>G	ENSP00000426541.2:p.Asn2668Asp
ENST00000512211.7:c.8002A>G	ENSP00000423828.3:p.Asn2668Asp
ENST00000257430.9:c.8002A>G MANE Select	ENSP00000257430.4:p.Asn2668Asp
ENST00000257430.8:c.8002A>G	ENSP00000257430.4:p.Asn2668Asp
ENST00000508376.6:c.8002A>G	ENSP00000427089.2:p.Asn2668Asp
ENST00000520401.1:c.231-13053A>G
NM_000038.5:c.8002A>G	NP_000029.2:p.Asn2668Asp
NM_001127510.2:c.8002A>G	NP_001120982.1:p.Asn2668Asp
NM_001127511.2:c.7948A>G	NP_001120983.2:p.Asn2650Asp
NM_001354895.1:c.8002A>G	NP_001341824.1:p.Asn2668Asp
NM_001354896.1:c.8056A>G	NP_001341825.1:p.Asn2686Asp
NM_001354897.1:c.8032A>G	NP_001341826.1:p.Asn2678Asp
NM_001354898.1:c.7927A>G	NP_001341827.1:p.Asn2643Asp
NM_001354899.1:c.7918A>G	NP_001341828.1:p.Asn2640Asp
NM_001354900.1:c.7879A>G	NP_001341829.1:p.Asn2627Asp
NM_001354901.1:c.7825A>G	NP_001341830.1:p.Asn2609Asp
NM_001354902.1:c.7729A>G	NP_001341831.1:p.Asn2577Asp
NM_001354903.1:c.7699A>G	NP_001341832.1:p.Asn2567Asp
NM_001354904.1:c.7624A>G	NP_001341833.1:p.Asn2542Asp
NM_001354905.1:c.7522A>G	NP_001341834.1:p.Asn2508Asp
NM_001354906.1:c.7153A>G	NP_001341835.1:p.Asn2385Asp
NM_000038.6:c.8002A>G MANE Select	NP_000029.2:p.Asn2668Asp
NM_001127510.3:c.8002A>G	NP_001120982.1:p.Asn2668Asp
NM_001127511.3:c.7948A>G	NP_001120983.2:p.Asn2650Asp
NM_001354895.2:c.8002A>G	NP_001341824.1:p.Asn2668Asp
NM_001354896.2:c.8056A>G	NP_001341825.1:p.Asn2686Asp
NM_001354897.2:c.8032A>G	NP_001341826.1:p.Asn2678Asp
NM_001354898.2:c.7927A>G	NP_001341827.1:p.Asn2643Asp
NM_001354899.2:c.7918A>G	NP_001341828.1:p.Asn2640Asp
NM_001354900.2:c.7879A>G	NP_001341829.1:p.Asn2627Asp
NM_001354901.2:c.7825A>G	NP_001341830.1:p.Asn2609Asp
NM_001354902.2:c.7729A>G	NP_001341831.1:p.Asn2577Asp
NM_001354903.2:c.7699A>G	NP_001341832.1:p.Asn2567Asp
NM_001354904.2:c.7624A>G	NP_001341833.1:p.Asn2542Asp
NM_001354905.2:c.7522A>G	NP_001341834.1:p.Asn2508Asp
NM_001354906.2:c.7153A>G	NP_001341835.1:p.Asn2385Asp