Canonical Allele Identifier: CA16037199

Gene: APC

Linked Data

• ClinVar Variation Id: 411540
• ClinVar RCV Id: RCV001026229 ; RCV003651891
• dbSNP Id: rs1060503363
• gnomAD v4: 5-112842880-C-G
• MyVariant Identifiers: chr5:g.112178577C>G (hg19) ; chr5:g.112842880C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112842880C>G , CM000667.2:g.112842880C>G	GRCh38
NC_000005.9:g.112178577C>G , CM000667.1:g.112178577C>G	GRCh37
NC_000005.8:g.112206476C>G	NCBI36
NG_008481.4:g.155360C>G , LRG_130:g.155360C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7340C>G	ENSP00000473355.2:p.Ser2447Cys
ENST00000505350.2:c.*7292C>G	ENSP00000481752.1:n.*7292C>G
ENST00000507379.6:c.7232C>G	ENSP00000423224.2:p.Ser2411Cys
ENST00000509732.6:c.7286C>G	ENSP00000426541.2:p.Ser2429Cys
ENST00000512211.7:c.7286C>G	ENSP00000423828.3:p.Ser2429Cys
ENST00000257430.9:c.7286C>G MANE Select	ENSP00000257430.4:p.Ser2429Cys
ENST00000257430.8:c.7286C>G	ENSP00000257430.4:p.Ser2429Cys
ENST00000508376.6:c.7286C>G	ENSP00000427089.2:p.Ser2429Cys
ENST00000520401.1:c.231-13769C>G
NM_000038.5:c.7286C>G	NP_000029.2:p.Ser2429Cys
NM_001127510.2:c.7286C>G	NP_001120982.1:p.Ser2429Cys
NM_001127511.2:c.7232C>G	NP_001120983.2:p.Ser2411Cys
NM_001354895.1:c.7286C>G	NP_001341824.1:p.Ser2429Cys
NM_001354896.1:c.7340C>G	NP_001341825.1:p.Ser2447Cys
NM_001354897.1:c.7316C>G	NP_001341826.1:p.Ser2439Cys
NM_001354898.1:c.7211C>G	NP_001341827.1:p.Ser2404Cys
NM_001354899.1:c.7202C>G	NP_001341828.1:p.Ser2401Cys
NM_001354900.1:c.7163C>G	NP_001341829.1:p.Ser2388Cys
NM_001354901.1:c.7109C>G	NP_001341830.1:p.Ser2370Cys
NM_001354902.1:c.7013C>G	NP_001341831.1:p.Ser2338Cys
NM_001354903.1:c.6983C>G	NP_001341832.1:p.Ser2328Cys
NM_001354904.1:c.6908C>G	NP_001341833.1:p.Ser2303Cys
NM_001354905.1:c.6806C>G	NP_001341834.1:p.Ser2269Cys
NM_001354906.1:c.6437C>G	NP_001341835.1:p.Ser2146Cys
NM_000038.6:c.7286C>G MANE Select	NP_000029.2:p.Ser2429Cys
NM_001127510.3:c.7286C>G	NP_001120982.1:p.Ser2429Cys
NM_001127511.3:c.7232C>G	NP_001120983.2:p.Ser2411Cys
NM_001354895.2:c.7286C>G	NP_001341824.1:p.Ser2429Cys
NM_001354896.2:c.7340C>G	NP_001341825.1:p.Ser2447Cys
NM_001354897.2:c.7316C>G	NP_001341826.1:p.Ser2439Cys
NM_001354898.2:c.7211C>G	NP_001341827.1:p.Ser2404Cys
NM_001354899.2:c.7202C>G	NP_001341828.1:p.Ser2401Cys
NM_001354900.2:c.7163C>G	NP_001341829.1:p.Ser2388Cys
NM_001354901.2:c.7109C>G	NP_001341830.1:p.Ser2370Cys
NM_001354902.2:c.7013C>G	NP_001341831.1:p.Ser2338Cys
NM_001354903.2:c.6983C>G	NP_001341832.1:p.Ser2328Cys
NM_001354904.2:c.6908C>G	NP_001341833.1:p.Ser2303Cys
NM_001354905.2:c.6806C>G	NP_001341834.1:p.Ser2269Cys
NM_001354906.2:c.6437C>G	NP_001341835.1:p.Ser2146Cys