Canonical Allele Identifier: CA16036776

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112178382T>C (hg19) ; chr5:g.112842685T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112842685T>C , CM000667.2:g.112842685T>C	GRCh38
NC_000005.9:g.112178382T>C , CM000667.1:g.112178382T>C	GRCh37
NC_000005.8:g.112206281T>C	NCBI36
NG_008481.4:g.155165T>C , LRG_130:g.155165T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7145T>C	ENSP00000473355.2:p.Met2382Thr
ENST00000505350.2:c.*7097T>C	ENSP00000481752.1:n.*7097T>C
ENST00000507379.6:c.7037T>C	ENSP00000423224.2:p.Met2346Thr
ENST00000509732.6:c.7091T>C	ENSP00000426541.2:p.Met2364Thr
ENST00000512211.7:c.7091T>C	ENSP00000423828.3:p.Met2364Thr
ENST00000257430.9:c.7091T>C MANE Select	ENSP00000257430.4:p.Met2364Thr
ENST00000257430.8:c.7091T>C	ENSP00000257430.4:p.Met2364Thr
ENST00000508376.6:c.7091T>C	ENSP00000427089.2:p.Met2364Thr
ENST00000508624.5:c.*6413T>C	ENSP00000424265.1:n.*6413T>C
ENST00000520401.1:c.230+13713T>C
NM_000038.5:c.7091T>C	NP_000029.2:p.Met2364Thr
NM_001127510.2:c.7091T>C	NP_001120982.1:p.Met2364Thr
NM_001127511.2:c.7037T>C	NP_001120983.2:p.Met2346Thr
NM_001354895.1:c.7091T>C	NP_001341824.1:p.Met2364Thr
NM_001354896.1:c.7145T>C	NP_001341825.1:p.Met2382Thr
NM_001354897.1:c.7121T>C	NP_001341826.1:p.Met2374Thr
NM_001354898.1:c.7016T>C	NP_001341827.1:p.Met2339Thr
NM_001354899.1:c.7007T>C	NP_001341828.1:p.Met2336Thr
NM_001354900.1:c.6968T>C	NP_001341829.1:p.Met2323Thr
NM_001354901.1:c.6914T>C	NP_001341830.1:p.Met2305Thr
NM_001354902.1:c.6818T>C	NP_001341831.1:p.Met2273Thr
NM_001354903.1:c.6788T>C	NP_001341832.1:p.Met2263Thr
NM_001354904.1:c.6713T>C	NP_001341833.1:p.Met2238Thr
NM_001354905.1:c.6611T>C	NP_001341834.1:p.Met2204Thr
NM_001354906.1:c.6242T>C	NP_001341835.1:p.Met2081Thr
NM_000038.6:c.7091T>C MANE Select	NP_000029.2:p.Met2364Thr
NM_001127510.3:c.7091T>C	NP_001120982.1:p.Met2364Thr
NM_001127511.3:c.7037T>C	NP_001120983.2:p.Met2346Thr
NM_001354895.2:c.7091T>C	NP_001341824.1:p.Met2364Thr
NM_001354896.2:c.7145T>C	NP_001341825.1:p.Met2382Thr
NM_001354897.2:c.7121T>C	NP_001341826.1:p.Met2374Thr
NM_001354898.2:c.7016T>C	NP_001341827.1:p.Met2339Thr
NM_001354899.2:c.7007T>C	NP_001341828.1:p.Met2336Thr
NM_001354900.2:c.6968T>C	NP_001341829.1:p.Met2323Thr
NM_001354901.2:c.6914T>C	NP_001341830.1:p.Met2305Thr
NM_001354902.2:c.6818T>C	NP_001341831.1:p.Met2273Thr
NM_001354903.2:c.6788T>C	NP_001341832.1:p.Met2263Thr
NM_001354904.2:c.6713T>C	NP_001341833.1:p.Met2238Thr
NM_001354905.2:c.6611T>C	NP_001341834.1:p.Met2204Thr
NM_001354906.2:c.6242T>C	NP_001341835.1:p.Met2081Thr