Canonical Allele Identifier: CA16038659

Gene: APC

Linked Data

• dbSNP Id: rs775012353
• MyVariant Identifiers: chr5:g.112179270G>C (hg19) ; chr5:g.112843573G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843573G>C , CM000667.2:g.112843573G>C	GRCh38
NC_000005.9:g.112179270G>C , CM000667.1:g.112179270G>C	GRCh37
NC_000005.8:g.112207169G>C	NCBI36
NG_008481.4:g.156053G>C , LRG_130:g.156053G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8033G>C	ENSP00000473355.2:p.Arg2678Thr
ENST00000505350.2:c.*7985G>C	ENSP00000481752.1:n.*7985G>C
ENST00000507379.6:c.7925G>C	ENSP00000423224.2:p.Arg2642Thr
ENST00000509732.6:c.7979G>C	ENSP00000426541.2:p.Arg2660Thr
ENST00000512211.7:c.7979G>C	ENSP00000423828.3:p.Arg2660Thr
ENST00000257430.9:c.7979G>C MANE Select	ENSP00000257430.4:p.Arg2660Thr
ENST00000257430.8:c.7979G>C	ENSP00000257430.4:p.Arg2660Thr
ENST00000508376.6:c.7979G>C	ENSP00000427089.2:p.Arg2660Thr
ENST00000520401.1:c.231-13076G>C
NM_000038.5:c.7979G>C	NP_000029.2:p.Arg2660Thr
NM_001127510.2:c.7979G>C	NP_001120982.1:p.Arg2660Thr
NM_001127511.2:c.7925G>C	NP_001120983.2:p.Arg2642Thr
NM_001354895.1:c.7979G>C	NP_001341824.1:p.Arg2660Thr
NM_001354896.1:c.8033G>C	NP_001341825.1:p.Arg2678Thr
NM_001354897.1:c.8009G>C	NP_001341826.1:p.Arg2670Thr
NM_001354898.1:c.7904G>C	NP_001341827.1:p.Arg2635Thr
NM_001354899.1:c.7895G>C	NP_001341828.1:p.Arg2632Thr
NM_001354900.1:c.7856G>C	NP_001341829.1:p.Arg2619Thr
NM_001354901.1:c.7802G>C	NP_001341830.1:p.Arg2601Thr
NM_001354902.1:c.7706G>C	NP_001341831.1:p.Arg2569Thr
NM_001354903.1:c.7676G>C	NP_001341832.1:p.Arg2559Thr
NM_001354904.1:c.7601G>C	NP_001341833.1:p.Arg2534Thr
NM_001354905.1:c.7499G>C	NP_001341834.1:p.Arg2500Thr
NM_001354906.1:c.7130G>C	NP_001341835.1:p.Arg2377Thr
NM_000038.6:c.7979G>C MANE Select	NP_000029.2:p.Arg2660Thr
NM_001127510.3:c.7979G>C	NP_001120982.1:p.Arg2660Thr
NM_001127511.3:c.7925G>C	NP_001120983.2:p.Arg2642Thr
NM_001354895.2:c.7979G>C	NP_001341824.1:p.Arg2660Thr
NM_001354896.2:c.8033G>C	NP_001341825.1:p.Arg2678Thr
NM_001354897.2:c.8009G>C	NP_001341826.1:p.Arg2670Thr
NM_001354898.2:c.7904G>C	NP_001341827.1:p.Arg2635Thr
NM_001354899.2:c.7895G>C	NP_001341828.1:p.Arg2632Thr
NM_001354900.2:c.7856G>C	NP_001341829.1:p.Arg2619Thr
NM_001354901.2:c.7802G>C	NP_001341830.1:p.Arg2601Thr
NM_001354902.2:c.7706G>C	NP_001341831.1:p.Arg2569Thr
NM_001354903.2:c.7676G>C	NP_001341832.1:p.Arg2559Thr
NM_001354904.2:c.7601G>C	NP_001341833.1:p.Arg2534Thr
NM_001354905.2:c.7499G>C	NP_001341834.1:p.Arg2500Thr
NM_001354906.2:c.7130G>C	NP_001341835.1:p.Arg2377Thr