Canonical Allele Identifier: CA16027976

Gene: APC

Linked Data

• dbSNP Id: rs2149882847
• MyVariant Identifiers: chr5:g.112174328C>G (hg19) ; chr5:g.112838631C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838631C>G , CM000667.2:g.112838631C>G	GRCh38
NC_000005.9:g.112174328C>G , CM000667.1:g.112174328C>G	GRCh37
NC_000005.8:g.112202227C>G	NCBI36
NG_008481.4:g.151111C>G , LRG_130:g.151111C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000502371.3:c.2702C>G	ENSP00000484935.2:n.2702C>G
ENST00000504915.3:c.3091C>G	ENSP00000473355.2:p.His1031Asp
ENST00000505350.2:c.*3043C>G	ENSP00000481752.1:n.*3043C>G
ENST00000507379.6:c.2983C>G	ENSP00000423224.2:p.His995Asp
ENST00000509732.6:c.3037C>G	ENSP00000426541.2:p.His1013Asp
ENST00000512211.7:c.3037C>G	ENSP00000423828.3:p.His1013Asp
ENST00000257430.9:c.3037C>G MANE Select	ENSP00000257430.4:p.His1013Asp
ENST00000257430.8:c.3037C>G	ENSP00000257430.4:p.His1013Asp
ENST00000502371.2:c.1390C>G
ENST00000507379.5:c.2983C>G	ENSP00000423224.1:p.His995Asp
ENST00000508376.6:c.3037C>G	ENSP00000427089.2:p.His1013Asp
ENST00000508624.5:c.*2359C>G	ENSP00000424265.1:n.*2359C>G
ENST00000512211.6:c.3037C>G	ENSP00000423828.2:p.His1013Asp
ENST00000520401.1:c.230+9659C>G
NM_000038.5:c.3037C>G	NP_000029.2:p.His1013Asp
NM_001127510.2:c.3037C>G	NP_001120982.1:p.His1013Asp
NM_001127511.2:c.2983C>G	NP_001120983.2:p.His995Asp
NM_001354895.1:c.3037C>G	NP_001341824.1:p.His1013Asp
NM_001354896.1:c.3091C>G	NP_001341825.1:p.His1031Asp
NM_001354897.1:c.3067C>G	NP_001341826.1:p.His1023Asp
NM_001354898.1:c.2962C>G	NP_001341827.1:p.His988Asp
NM_001354899.1:c.2953C>G	NP_001341828.1:p.His985Asp
NM_001354900.1:c.2914C>G	NP_001341829.1:p.His972Asp
NM_001354901.1:c.2860C>G	NP_001341830.1:p.His954Asp
NM_001354902.1:c.2764C>G	NP_001341831.1:p.His922Asp
NM_001354903.1:c.2734C>G	NP_001341832.1:p.His912Asp
NM_001354904.1:c.2659C>G	NP_001341833.1:p.His887Asp
NM_001354905.1:c.2557C>G	NP_001341834.1:p.His853Asp
NM_001354906.1:c.2188C>G	NP_001341835.1:p.His730Asp
NM_000038.6:c.3037C>G MANE Select	NP_000029.2:p.His1013Asp
NM_001127510.3:c.3037C>G	NP_001120982.1:p.His1013Asp
NM_001127511.3:c.2983C>G	NP_001120983.2:p.His995Asp
NM_001354895.2:c.3037C>G	NP_001341824.1:p.His1013Asp
NM_001354896.2:c.3091C>G	NP_001341825.1:p.His1031Asp
NM_001354897.2:c.3067C>G	NP_001341826.1:p.His1023Asp
NM_001354898.2:c.2962C>G	NP_001341827.1:p.His988Asp
NM_001354899.2:c.2953C>G	NP_001341828.1:p.His985Asp
NM_001354900.2:c.2914C>G	NP_001341829.1:p.His972Asp
NM_001354901.2:c.2860C>G	NP_001341830.1:p.His954Asp
NM_001354902.2:c.2764C>G	NP_001341831.1:p.His922Asp
NM_001354903.2:c.2734C>G	NP_001341832.1:p.His912Asp
NM_001354904.2:c.2659C>G	NP_001341833.1:p.His887Asp
NM_001354905.2:c.2557C>G	NP_001341834.1:p.His853Asp
NM_001354906.2:c.2188C>G	NP_001341835.1:p.His730Asp