Canonical Allele Identifier: CA16038043

Gene: APC

Linked Data

• dbSNP Id: rs2149992051
• MyVariant Identifiers: chr5:g.112178985G>C (hg19) ; chr5:g.112843288G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843288G>C , CM000667.2:g.112843288G>C	GRCh38
NC_000005.9:g.112178985G>C , CM000667.1:g.112178985G>C	GRCh37
NC_000005.8:g.112206884G>C	NCBI36
NG_008481.4:g.155768G>C , LRG_130:g.155768G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7748G>C	ENSP00000473355.2:p.Arg2583Thr
ENST00000505350.2:c.*7700G>C	ENSP00000481752.1:n.*7700G>C
ENST00000507379.6:c.7640G>C	ENSP00000423224.2:p.Arg2547Thr
ENST00000509732.6:c.7694G>C	ENSP00000426541.2:p.Arg2565Thr
ENST00000512211.7:c.7694G>C	ENSP00000423828.3:p.Arg2565Thr
ENST00000257430.9:c.7694G>C MANE Select	ENSP00000257430.4:p.Arg2565Thr
ENST00000257430.8:c.7694G>C	ENSP00000257430.4:p.Arg2565Thr
ENST00000508376.6:c.7694G>C	ENSP00000427089.2:p.Arg2565Thr
ENST00000520401.1:c.231-13361G>C
NM_000038.5:c.7694G>C	NP_000029.2:p.Arg2565Thr
NM_001127510.2:c.7694G>C	NP_001120982.1:p.Arg2565Thr
NM_001127511.2:c.7640G>C	NP_001120983.2:p.Arg2547Thr
NM_001354895.1:c.7694G>C	NP_001341824.1:p.Arg2565Thr
NM_001354896.1:c.7748G>C	NP_001341825.1:p.Arg2583Thr
NM_001354897.1:c.7724G>C	NP_001341826.1:p.Arg2575Thr
NM_001354898.1:c.7619G>C	NP_001341827.1:p.Arg2540Thr
NM_001354899.1:c.7610G>C	NP_001341828.1:p.Arg2537Thr
NM_001354900.1:c.7571G>C	NP_001341829.1:p.Arg2524Thr
NM_001354901.1:c.7517G>C	NP_001341830.1:p.Arg2506Thr
NM_001354902.1:c.7421G>C	NP_001341831.1:p.Arg2474Thr
NM_001354903.1:c.7391G>C	NP_001341832.1:p.Arg2464Thr
NM_001354904.1:c.7316G>C	NP_001341833.1:p.Arg2439Thr
NM_001354905.1:c.7214G>C	NP_001341834.1:p.Arg2405Thr
NM_001354906.1:c.6845G>C	NP_001341835.1:p.Arg2282Thr
NM_000038.6:c.7694G>C MANE Select	NP_000029.2:p.Arg2565Thr
NM_001127510.3:c.7694G>C	NP_001120982.1:p.Arg2565Thr
NM_001127511.3:c.7640G>C	NP_001120983.2:p.Arg2547Thr
NM_001354895.2:c.7694G>C	NP_001341824.1:p.Arg2565Thr
NM_001354896.2:c.7748G>C	NP_001341825.1:p.Arg2583Thr
NM_001354897.2:c.7724G>C	NP_001341826.1:p.Arg2575Thr
NM_001354898.2:c.7619G>C	NP_001341827.1:p.Arg2540Thr
NM_001354899.2:c.7610G>C	NP_001341828.1:p.Arg2537Thr
NM_001354900.2:c.7571G>C	NP_001341829.1:p.Arg2524Thr
NM_001354901.2:c.7517G>C	NP_001341830.1:p.Arg2506Thr
NM_001354902.2:c.7421G>C	NP_001341831.1:p.Arg2474Thr
NM_001354903.2:c.7391G>C	NP_001341832.1:p.Arg2464Thr
NM_001354904.2:c.7316G>C	NP_001341833.1:p.Arg2439Thr
NM_001354905.2:c.7214G>C	NP_001341834.1:p.Arg2405Thr
NM_001354906.2:c.6845G>C	NP_001341835.1:p.Arg2282Thr