Canonical Allele Identifier: CA16038180

Gene: APC

Linked Data

• dbSNP Id: rs199806334
• MyVariant Identifiers: chr5:g.112179048G>C (hg19) ; chr5:g.112843351G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843351G>C , CM000667.2:g.112843351G>C	GRCh38
NC_000005.9:g.112179048G>C , CM000667.1:g.112179048G>C	GRCh37
NC_000005.8:g.112206947G>C	NCBI36
NG_008481.4:g.155831G>C , LRG_130:g.155831G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7811G>C	ENSP00000473355.2:p.Ser2604Thr
ENST00000505350.2:c.*7763G>C	ENSP00000481752.1:n.*7763G>C
ENST00000507379.6:c.7703G>C	ENSP00000423224.2:p.Ser2568Thr
ENST00000509732.6:c.7757G>C	ENSP00000426541.2:p.Ser2586Thr
ENST00000512211.7:c.7757G>C	ENSP00000423828.3:p.Ser2586Thr
ENST00000257430.9:c.7757G>C MANE Select	ENSP00000257430.4:p.Ser2586Thr
ENST00000257430.8:c.7757G>C	ENSP00000257430.4:p.Ser2586Thr
ENST00000508376.6:c.7757G>C	ENSP00000427089.2:p.Ser2586Thr
ENST00000520401.1:c.231-13298G>C
NM_000038.5:c.7757G>C	NP_000029.2:p.Ser2586Thr
NM_001127510.2:c.7757G>C	NP_001120982.1:p.Ser2586Thr
NM_001127511.2:c.7703G>C	NP_001120983.2:p.Ser2568Thr
NM_001354895.1:c.7757G>C	NP_001341824.1:p.Ser2586Thr
NM_001354896.1:c.7811G>C	NP_001341825.1:p.Ser2604Thr
NM_001354897.1:c.7787G>C	NP_001341826.1:p.Ser2596Thr
NM_001354898.1:c.7682G>C	NP_001341827.1:p.Ser2561Thr
NM_001354899.1:c.7673G>C	NP_001341828.1:p.Ser2558Thr
NM_001354900.1:c.7634G>C	NP_001341829.1:p.Ser2545Thr
NM_001354901.1:c.7580G>C	NP_001341830.1:p.Ser2527Thr
NM_001354902.1:c.7484G>C	NP_001341831.1:p.Ser2495Thr
NM_001354903.1:c.7454G>C	NP_001341832.1:p.Ser2485Thr
NM_001354904.1:c.7379G>C	NP_001341833.1:p.Ser2460Thr
NM_001354905.1:c.7277G>C	NP_001341834.1:p.Ser2426Thr
NM_001354906.1:c.6908G>C	NP_001341835.1:p.Ser2303Thr
NM_000038.6:c.7757G>C MANE Select	NP_000029.2:p.Ser2586Thr
NM_001127510.3:c.7757G>C	NP_001120982.1:p.Ser2586Thr
NM_001127511.3:c.7703G>C	NP_001120983.2:p.Ser2568Thr
NM_001354895.2:c.7757G>C	NP_001341824.1:p.Ser2586Thr
NM_001354896.2:c.7811G>C	NP_001341825.1:p.Ser2604Thr
NM_001354897.2:c.7787G>C	NP_001341826.1:p.Ser2596Thr
NM_001354898.2:c.7682G>C	NP_001341827.1:p.Ser2561Thr
NM_001354899.2:c.7673G>C	NP_001341828.1:p.Ser2558Thr
NM_001354900.2:c.7634G>C	NP_001341829.1:p.Ser2545Thr
NM_001354901.2:c.7580G>C	NP_001341830.1:p.Ser2527Thr
NM_001354902.2:c.7484G>C	NP_001341831.1:p.Ser2495Thr
NM_001354903.2:c.7454G>C	NP_001341832.1:p.Ser2485Thr
NM_001354904.2:c.7379G>C	NP_001341833.1:p.Ser2460Thr
NM_001354905.2:c.7277G>C	NP_001341834.1:p.Ser2426Thr
NM_001354906.2:c.6908G>C	NP_001341835.1:p.Ser2303Thr