Canonical Allele Identifier: CA16038748

Gene: APC

Linked Data

• ClinVar Variation Id: 3069608
• ClinVar RCV Id: RCV004008152 ; RCV004371939
• dbSNP Id: rs2149998000
• MyVariant Identifiers: chr5:g.112179310A>C (hg19) ; chr5:g.112843613A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843613A>C , CM000667.2:g.112843613A>C	GRCh38
NC_000005.9:g.112179310A>C , CM000667.1:g.112179310A>C	GRCh37
NC_000005.8:g.112207209A>C	NCBI36
NG_008481.4:g.156093A>C , LRG_130:g.156093A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8073A>C	ENSP00000473355.2:p.Arg2691Ser
ENST00000505350.2:c.*8025A>C	ENSP00000481752.1:n.*8025A>C
ENST00000507379.6:c.7965A>C	ENSP00000423224.2:p.Arg2655Ser
ENST00000509732.6:c.8019A>C	ENSP00000426541.2:p.Arg2673Ser
ENST00000512211.7:c.8019A>C	ENSP00000423828.3:p.Arg2673Ser
ENST00000257430.9:c.8019A>C MANE Select	ENSP00000257430.4:p.Arg2673Ser
ENST00000257430.8:c.8019A>C	ENSP00000257430.4:p.Arg2673Ser
ENST00000508376.6:c.8019A>C	ENSP00000427089.2:p.Arg2673Ser
ENST00000520401.1:c.231-13036A>C
NM_000038.5:c.8019A>C	NP_000029.2:p.Arg2673Ser
NM_001127510.2:c.8019A>C	NP_001120982.1:p.Arg2673Ser
NM_001127511.2:c.7965A>C	NP_001120983.2:p.Arg2655Ser
NM_001354895.1:c.8019A>C	NP_001341824.1:p.Arg2673Ser
NM_001354896.1:c.8073A>C	NP_001341825.1:p.Arg2691Ser
NM_001354897.1:c.8049A>C	NP_001341826.1:p.Arg2683Ser
NM_001354898.1:c.7944A>C	NP_001341827.1:p.Arg2648Ser
NM_001354899.1:c.7935A>C	NP_001341828.1:p.Arg2645Ser
NM_001354900.1:c.7896A>C	NP_001341829.1:p.Arg2632Ser
NM_001354901.1:c.7842A>C	NP_001341830.1:p.Arg2614Ser
NM_001354902.1:c.7746A>C	NP_001341831.1:p.Arg2582Ser
NM_001354903.1:c.7716A>C	NP_001341832.1:p.Arg2572Ser
NM_001354904.1:c.7641A>C	NP_001341833.1:p.Arg2547Ser
NM_001354905.1:c.7539A>C	NP_001341834.1:p.Arg2513Ser
NM_001354906.1:c.7170A>C	NP_001341835.1:p.Arg2390Ser
NM_000038.6:c.8019A>C MANE Select	NP_000029.2:p.Arg2673Ser
NM_001127510.3:c.8019A>C	NP_001120982.1:p.Arg2673Ser
NM_001127511.3:c.7965A>C	NP_001120983.2:p.Arg2655Ser
NM_001354895.2:c.8019A>C	NP_001341824.1:p.Arg2673Ser
NM_001354896.2:c.8073A>C	NP_001341825.1:p.Arg2691Ser
NM_001354897.2:c.8049A>C	NP_001341826.1:p.Arg2683Ser
NM_001354898.2:c.7944A>C	NP_001341827.1:p.Arg2648Ser
NM_001354899.2:c.7935A>C	NP_001341828.1:p.Arg2645Ser
NM_001354900.2:c.7896A>C	NP_001341829.1:p.Arg2632Ser
NM_001354901.2:c.7842A>C	NP_001341830.1:p.Arg2614Ser
NM_001354902.2:c.7746A>C	NP_001341831.1:p.Arg2582Ser
NM_001354903.2:c.7716A>C	NP_001341832.1:p.Arg2572Ser
NM_001354904.2:c.7641A>C	NP_001341833.1:p.Arg2547Ser
NM_001354905.2:c.7539A>C	NP_001341834.1:p.Arg2513Ser
NM_001354906.2:c.7170A>C	NP_001341835.1:p.Arg2390Ser