Canonical Allele Identifier: CA16023222

Gene: APC

Linked Data

• dbSNP Id: rs863224289
• MyVariant Identifiers: chr5:g.112151227T>G (hg19) ; chr5:g.112815530T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112815530T>G , CM000667.2:g.112815530T>G	GRCh38
NC_000005.9:g.112151227T>G , CM000667.1:g.112151227T>G	GRCh37
NC_000005.8:g.112179126T>G	NCBI36
NG_008481.4:g.128010T>G , LRG_130:g.128010T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.870T>G	ENSP00000484935.2:p.Ser290Arg
ENST00000504915.3:c.870T>G	ENSP00000473355.2:p.Ser290Arg
ENST00000505084.2:n.926T>G
ENST00000505350.2:c.*876T>G	ENSP00000481752.1:n.*876T>G
ENST00000507379.6:c.816T>G	ENSP00000423224.2:p.Ser272Arg
ENST00000509732.6:c.870T>G	ENSP00000426541.2:p.Ser290Arg
ENST00000512211.7:c.870T>G	ENSP00000423828.3:p.Ser290Arg
ENST00000257430.9:c.870T>G MANE Select	ENSP00000257430.4:p.Ser290Arg
ENST00000257430.8:c.870T>G	ENSP00000257430.4:p.Ser290Arg
ENST00000507379.5:c.816T>G	ENSP00000423224.1:p.Ser272Arg
ENST00000508376.6:c.870T>G	ENSP00000427089.2:p.Ser290Arg
ENST00000508624.5:c.*192T>G	ENSP00000424265.1:n.*192T>G
ENST00000512211.6:c.870T>G	ENSP00000423828.2:p.Ser290Arg
NM_000038.5:c.870T>G	NP_000029.2:p.Ser290Arg
NM_001127510.2:c.870T>G	NP_001120982.1:p.Ser290Arg
NM_001127511.2:c.816T>G	NP_001120983.2:p.Ser272Arg
NM_001354895.1:c.870T>G	NP_001341824.1:p.Ser290Arg
NM_001354896.1:c.870T>G	NP_001341825.1:p.Ser290Arg
NM_001354897.1:c.900T>G	NP_001341826.1:p.Ser300Arg
NM_001354898.1:c.795T>G	NP_001341827.1:p.Ser265Arg
NM_001354899.1:c.786T>G	NP_001341828.1:p.Ser262Arg
NM_001354900.1:c.693T>G	NP_001341829.1:p.Ser231Arg
NM_001354901.1:c.693T>G	NP_001341830.1:p.Ser231Arg
NM_001354902.1:c.900T>G	NP_001341831.1:p.Ser300Arg
NM_001354903.1:c.870T>G	NP_001341832.1:p.Ser290Arg
NM_001354904.1:c.795T>G	NP_001341833.1:p.Ser265Arg
NM_001354905.1:c.693T>G	NP_001341834.1:p.Ser231Arg
NM_001354906.1:c.21T>G	NP_001341835.1:p.Ser7Arg
NM_000038.6:c.870T>G MANE Select	NP_000029.2:p.Ser290Arg
NM_001127510.3:c.870T>G	NP_001120982.1:p.Ser290Arg
NM_001127511.3:c.816T>G	NP_001120983.2:p.Ser272Arg
NM_001354895.2:c.870T>G	NP_001341824.1:p.Ser290Arg
NM_001354896.2:c.870T>G	NP_001341825.1:p.Ser290Arg
NM_001354897.2:c.900T>G	NP_001341826.1:p.Ser300Arg
NM_001354898.2:c.795T>G	NP_001341827.1:p.Ser265Arg
NM_001354899.2:c.786T>G	NP_001341828.1:p.Ser262Arg
NM_001354900.2:c.693T>G	NP_001341829.1:p.Ser231Arg
NM_001354901.2:c.693T>G	NP_001341830.1:p.Ser231Arg
NM_001354902.2:c.900T>G	NP_001341831.1:p.Ser300Arg
NM_001354903.2:c.870T>G	NP_001341832.1:p.Ser290Arg
NM_001354904.2:c.795T>G	NP_001341833.1:p.Ser265Arg
NM_001354905.2:c.693T>G	NP_001341834.1:p.Ser231Arg
NM_001354906.2:c.21T>G	NP_001341835.1:p.Ser7Arg