Canonical Allele Identifier: CA16024533

Gene: APC

Linked Data

• MyVariant Identifiers: chr5:g.112162870C>G (hg19) ; chr5:g.112827173C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112827173C>G , CM000667.2:g.112827173C>G	GRCh38
NC_000005.9:g.112162870C>G , CM000667.1:g.112162870C>G	GRCh37
NC_000005.8:g.112190769C>G	NCBI36
NG_008481.4:g.139653C>G , LRG_130:g.139653C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.1408+5182C>G	ENSP00000484935.2:n.1408+5182C>G
ENST00000504915.3:c.1528C>G	ENSP00000473355.2:p.His510Asp
ENST00000505084.2:n.1530C>G
ENST00000505350.2:c.*1480C>G	ENSP00000481752.1:n.*1480C>G
ENST00000507379.6:c.1420C>G	ENSP00000423224.2:p.His474Asp
ENST00000509732.6:c.1474C>G	ENSP00000426541.2:p.His492Asp
ENST00000512211.7:c.1474C>G	ENSP00000423828.3:p.His492Asp
ENST00000257430.9:c.1474C>G MANE Select	ENSP00000257430.4:p.His492Asp
ENST00000257430.8:c.1474C>G	ENSP00000257430.4:p.His492Asp
ENST00000502371.2:c.96+5182C>G
ENST00000504915.2:c.163C>G	ENSP00000473355.1:p.His55Asp
ENST00000507379.5:c.1420C>G	ENSP00000423224.1:p.His474Asp
ENST00000508376.6:c.1474C>G	ENSP00000427089.2:p.His492Asp
ENST00000508624.5:c.*796C>G	ENSP00000424265.1:n.*796C>G
ENST00000512211.6:c.1474C>G	ENSP00000423828.2:p.His492Asp
NM_000038.5:c.1474C>G	NP_000029.2:p.His492Asp
NM_001127510.2:c.1474C>G	NP_001120982.1:p.His492Asp
NM_001127511.2:c.1420C>G	NP_001120983.2:p.His474Asp
NM_001354895.1:c.1474C>G	NP_001341824.1:p.His492Asp
NM_001354896.1:c.1528C>G	NP_001341825.1:p.His510Asp
NM_001354897.1:c.1504C>G	NP_001341826.1:p.His502Asp
NM_001354898.1:c.1399C>G	NP_001341827.1:p.His467Asp
NM_001354899.1:c.1390C>G	NP_001341828.1:p.His464Asp
NM_001354900.1:c.1351C>G	NP_001341829.1:p.His451Asp
NM_001354901.1:c.1297C>G	NP_001341830.1:p.His433Asp
NM_001354902.1:c.1201C>G	NP_001341831.1:p.His401Asp
NM_001354903.1:c.1171C>G	NP_001341832.1:p.His391Asp
NM_001354904.1:c.1096C>G	NP_001341833.1:p.His366Asp
NM_001354905.1:c.994C>G	NP_001341834.1:p.His332Asp
NM_001354906.1:c.625C>G	NP_001341835.1:p.His209Asp
NM_000038.6:c.1474C>G MANE Select	NP_000029.2:p.His492Asp
NM_001127510.3:c.1474C>G	NP_001120982.1:p.His492Asp
NM_001127511.3:c.1420C>G	NP_001120983.2:p.His474Asp
NM_001354895.2:c.1474C>G	NP_001341824.1:p.His492Asp
NM_001354896.2:c.1528C>G	NP_001341825.1:p.His510Asp
NM_001354897.2:c.1504C>G	NP_001341826.1:p.His502Asp
NM_001354898.2:c.1399C>G	NP_001341827.1:p.His467Asp
NM_001354899.2:c.1390C>G	NP_001341828.1:p.His464Asp
NM_001354900.2:c.1351C>G	NP_001341829.1:p.His451Asp
NM_001354901.2:c.1297C>G	NP_001341830.1:p.His433Asp
NM_001354902.2:c.1201C>G	NP_001341831.1:p.His401Asp
NM_001354903.2:c.1171C>G	NP_001341832.1:p.His391Asp
NM_001354904.2:c.1096C>G	NP_001341833.1:p.His366Asp
NM_001354905.2:c.994C>G	NP_001341834.1:p.His332Asp
NM_001354906.2:c.625C>G	NP_001341835.1:p.His209Asp