Canonical Allele Identifier: CA446211032

Gene: APC

Linked Data

• dbSNP Id: rs2149998232
• MyVariant Identifiers: chr5:g.112179328T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843631T>C , CM000667.2:g.112843631T>C	GRCh38
NC_000005.9:g.112179328T>C , CM000667.1:g.112179328T>C	GRCh37
NC_000005.8:g.112207227T>C	NCBI36
NG_008481.4:g.156111T>C , LRG_130:g.156111T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.8091T>C	ENSP00000473355.2:p.Thr2697=
ENST00000505350.2:c.*8043T>C	ENSP00000481752.1:n.*8043T>C
ENST00000507379.6:c.7983T>C	ENSP00000423224.2:p.Thr2661=
ENST00000509732.6:c.8037T>C	ENSP00000426541.2:p.Thr2679=
ENST00000512211.7:c.8037T>C	ENSP00000423828.3:p.Thr2679=
ENST00000257430.9:c.8037T>C MANE Select	ENSP00000257430.4:p.Thr2679=
ENST00000257430.8:c.8037T>C	ENSP00000257430.4:p.Thr2679=
ENST00000508376.6:c.8037T>C	ENSP00000427089.2:p.Thr2679=
ENST00000520401.1:c.231-13018T>C
NM_000038.5:c.8037T>C	NP_000029.2:p.Thr2679=
NM_001127510.2:c.8037T>C	NP_001120982.1:p.Thr2679=
NM_001127511.2:c.7983T>C	NP_001120983.2:p.Thr2661=
NM_001354895.1:c.8037T>C	NP_001341824.1:p.Thr2679=
NM_001354896.1:c.8091T>C	NP_001341825.1:p.Thr2697=
NM_001354897.1:c.8067T>C	NP_001341826.1:p.Thr2689=
NM_001354898.1:c.7962T>C	NP_001341827.1:p.Thr2654=
NM_001354899.1:c.7953T>C	NP_001341828.1:p.Thr2651=
NM_001354900.1:c.7914T>C	NP_001341829.1:p.Thr2638=
NM_001354901.1:c.7860T>C	NP_001341830.1:p.Thr2620=
NM_001354902.1:c.7764T>C	NP_001341831.1:p.Thr2588=
NM_001354903.1:c.7734T>C	NP_001341832.1:p.Thr2578=
NM_001354904.1:c.7659T>C	NP_001341833.1:p.Thr2553=
NM_001354905.1:c.7557T>C	NP_001341834.1:p.Thr2519=
NM_001354906.1:c.7188T>C	NP_001341835.1:p.Thr2396=
NM_000038.6:c.8037T>C MANE Select	NP_000029.2:p.Thr2679=
NM_001127510.3:c.8037T>C	NP_001120982.1:p.Thr2679=
NM_001127511.3:c.7983T>C	NP_001120983.2:p.Thr2661=
NM_001354895.2:c.8037T>C	NP_001341824.1:p.Thr2679=
NM_001354896.2:c.8091T>C	NP_001341825.1:p.Thr2697=
NM_001354897.2:c.8067T>C	NP_001341826.1:p.Thr2689=
NM_001354898.2:c.7962T>C	NP_001341827.1:p.Thr2654=
NM_001354899.2:c.7953T>C	NP_001341828.1:p.Thr2651=
NM_001354900.2:c.7914T>C	NP_001341829.1:p.Thr2638=
NM_001354901.2:c.7860T>C	NP_001341830.1:p.Thr2620=
NM_001354902.2:c.7764T>C	NP_001341831.1:p.Thr2588=
NM_001354903.2:c.7734T>C	NP_001341832.1:p.Thr2578=
NM_001354904.2:c.7659T>C	NP_001341833.1:p.Thr2553=
NM_001354905.2:c.7557T>C	NP_001341834.1:p.Thr2519=
NM_001354906.2:c.7188T>C	NP_001341835.1:p.Thr2396=