Canonical Allele Identifier: CA16038634

Gene: APC

Linked Data

• ClinVar Variation Id: 495374
• ClinVar RCV Id: RCV000587099 ; RCV001185311 ; RCV002530881 ; RCV003538394 ; RCV004002391
• dbSNP Id: rs1463203731
• gnomAD v4: 5-112843561-A-G
• MyVariant Identifiers: chr5:g.112179258A>G (hg19) ; chr5:g.112843561A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843561A>G , CM000667.2:g.112843561A>G	GRCh38
NC_000005.9:g.112179258A>G , CM000667.1:g.112179258A>G	GRCh37
NC_000005.8:g.112207157A>G	NCBI36
NG_008481.4:g.156041A>G , LRG_130:g.156041A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8021A>G	ENSP00000473355.2:p.Asp2674Gly
ENST00000505350.2:c.*7973A>G	ENSP00000481752.1:n.*7973A>G
ENST00000507379.6:c.7913A>G	ENSP00000423224.2:p.Asp2638Gly
ENST00000509732.6:c.7967A>G	ENSP00000426541.2:p.Asp2656Gly
ENST00000512211.7:c.7967A>G	ENSP00000423828.3:p.Asp2656Gly
ENST00000257430.9:c.7967A>G MANE Select	ENSP00000257430.4:p.Asp2656Gly
ENST00000257430.8:c.7967A>G	ENSP00000257430.4:p.Asp2656Gly
ENST00000508376.6:c.7967A>G	ENSP00000427089.2:p.Asp2656Gly
ENST00000520401.1:c.231-13088A>G
NM_000038.5:c.7967A>G	NP_000029.2:p.Asp2656Gly
NM_001127510.2:c.7967A>G	NP_001120982.1:p.Asp2656Gly
NM_001127511.2:c.7913A>G	NP_001120983.2:p.Asp2638Gly
NM_001354895.1:c.7967A>G	NP_001341824.1:p.Asp2656Gly
NM_001354896.1:c.8021A>G	NP_001341825.1:p.Asp2674Gly
NM_001354897.1:c.7997A>G	NP_001341826.1:p.Asp2666Gly
NM_001354898.1:c.7892A>G	NP_001341827.1:p.Asp2631Gly
NM_001354899.1:c.7883A>G	NP_001341828.1:p.Asp2628Gly
NM_001354900.1:c.7844A>G	NP_001341829.1:p.Asp2615Gly
NM_001354901.1:c.7790A>G	NP_001341830.1:p.Asp2597Gly
NM_001354902.1:c.7694A>G	NP_001341831.1:p.Asp2565Gly
NM_001354903.1:c.7664A>G	NP_001341832.1:p.Asp2555Gly
NM_001354904.1:c.7589A>G	NP_001341833.1:p.Asp2530Gly
NM_001354905.1:c.7487A>G	NP_001341834.1:p.Asp2496Gly
NM_001354906.1:c.7118A>G	NP_001341835.1:p.Asp2373Gly
NM_000038.6:c.7967A>G MANE Select	NP_000029.2:p.Asp2656Gly
NM_001127510.3:c.7967A>G	NP_001120982.1:p.Asp2656Gly
NM_001127511.3:c.7913A>G	NP_001120983.2:p.Asp2638Gly
NM_001354895.2:c.7967A>G	NP_001341824.1:p.Asp2656Gly
NM_001354896.2:c.8021A>G	NP_001341825.1:p.Asp2674Gly
NM_001354897.2:c.7997A>G	NP_001341826.1:p.Asp2666Gly
NM_001354898.2:c.7892A>G	NP_001341827.1:p.Asp2631Gly
NM_001354899.2:c.7883A>G	NP_001341828.1:p.Asp2628Gly
NM_001354900.2:c.7844A>G	NP_001341829.1:p.Asp2615Gly
NM_001354901.2:c.7790A>G	NP_001341830.1:p.Asp2597Gly
NM_001354902.2:c.7694A>G	NP_001341831.1:p.Asp2565Gly
NM_001354903.2:c.7664A>G	NP_001341832.1:p.Asp2555Gly
NM_001354904.2:c.7589A>G	NP_001341833.1:p.Asp2530Gly
NM_001354905.2:c.7487A>G	NP_001341834.1:p.Asp2496Gly
NM_001354906.2:c.7118A>G	NP_001341835.1:p.Asp2373Gly