Canonical Allele Identifier: CA16038050

Gene: APC

Linked Data

• ClinVar Variation Id: 2677331
• ClinVar RCV Id: RCV003476579
• dbSNP Id: rs2149992109
• MyVariant Identifiers: chr5:g.112178988G>C (hg19) ; chr5:g.112843291G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843291G>C , CM000667.2:g.112843291G>C	GRCh38
NC_000005.9:g.112178988G>C , CM000667.1:g.112178988G>C	GRCh37
NC_000005.8:g.112206887G>C	NCBI36
NG_008481.4:g.155771G>C , LRG_130:g.155771G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7751G>C	ENSP00000473355.2:p.Arg2584Thr
ENST00000505350.2:c.*7703G>C	ENSP00000481752.1:n.*7703G>C
ENST00000507379.6:c.7643G>C	ENSP00000423224.2:p.Arg2548Thr
ENST00000509732.6:c.7697G>C	ENSP00000426541.2:p.Arg2566Thr
ENST00000512211.7:c.7697G>C	ENSP00000423828.3:p.Arg2566Thr
ENST00000257430.9:c.7697G>C MANE Select	ENSP00000257430.4:p.Arg2566Thr
ENST00000257430.8:c.7697G>C	ENSP00000257430.4:p.Arg2566Thr
ENST00000508376.6:c.7697G>C	ENSP00000427089.2:p.Arg2566Thr
ENST00000520401.1:c.231-13358G>C
NM_000038.5:c.7697G>C	NP_000029.2:p.Arg2566Thr
NM_001127510.2:c.7697G>C	NP_001120982.1:p.Arg2566Thr
NM_001127511.2:c.7643G>C	NP_001120983.2:p.Arg2548Thr
NM_001354895.1:c.7697G>C	NP_001341824.1:p.Arg2566Thr
NM_001354896.1:c.7751G>C	NP_001341825.1:p.Arg2584Thr
NM_001354897.1:c.7727G>C	NP_001341826.1:p.Arg2576Thr
NM_001354898.1:c.7622G>C	NP_001341827.1:p.Arg2541Thr
NM_001354899.1:c.7613G>C	NP_001341828.1:p.Arg2538Thr
NM_001354900.1:c.7574G>C	NP_001341829.1:p.Arg2525Thr
NM_001354901.1:c.7520G>C	NP_001341830.1:p.Arg2507Thr
NM_001354902.1:c.7424G>C	NP_001341831.1:p.Arg2475Thr
NM_001354903.1:c.7394G>C	NP_001341832.1:p.Arg2465Thr
NM_001354904.1:c.7319G>C	NP_001341833.1:p.Arg2440Thr
NM_001354905.1:c.7217G>C	NP_001341834.1:p.Arg2406Thr
NM_001354906.1:c.6848G>C	NP_001341835.1:p.Arg2283Thr
NM_000038.6:c.7697G>C MANE Select	NP_000029.2:p.Arg2566Thr
NM_001127510.3:c.7697G>C	NP_001120982.1:p.Arg2566Thr
NM_001127511.3:c.7643G>C	NP_001120983.2:p.Arg2548Thr
NM_001354895.2:c.7697G>C	NP_001341824.1:p.Arg2566Thr
NM_001354896.2:c.7751G>C	NP_001341825.1:p.Arg2584Thr
NM_001354897.2:c.7727G>C	NP_001341826.1:p.Arg2576Thr
NM_001354898.2:c.7622G>C	NP_001341827.1:p.Arg2541Thr
NM_001354899.2:c.7613G>C	NP_001341828.1:p.Arg2538Thr
NM_001354900.2:c.7574G>C	NP_001341829.1:p.Arg2525Thr
NM_001354901.2:c.7520G>C	NP_001341830.1:p.Arg2507Thr
NM_001354902.2:c.7424G>C	NP_001341831.1:p.Arg2475Thr
NM_001354903.2:c.7394G>C	NP_001341832.1:p.Arg2465Thr
NM_001354904.2:c.7319G>C	NP_001341833.1:p.Arg2440Thr
NM_001354905.2:c.7217G>C	NP_001341834.1:p.Arg2406Thr
NM_001354906.2:c.6848G>C	NP_001341835.1:p.Arg2283Thr