Canonical Allele Identifier: CA16027927

Gene: APC

Linked Data

• dbSNP Id: rs879253876
• MyVariant Identifiers: chr5:g.112174307C>G (hg19) ; chr5:g.112838610C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112838610C>G , CM000667.2:g.112838610C>G	GRCh38
NC_000005.9:g.112174307C>G , CM000667.1:g.112174307C>G	GRCh37
NC_000005.8:g.112202206C>G	NCBI36
NG_008481.4:g.151090C>G , LRG_130:g.151090C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000502371.3:c.2681C>G	ENSP00000484935.2:n.2681C>G
ENST00000504915.3:c.3070C>G	ENSP00000473355.2:p.His1024Asp
ENST00000505350.2:c.*3022C>G	ENSP00000481752.1:n.*3022C>G
ENST00000507379.6:c.2962C>G	ENSP00000423224.2:p.His988Asp
ENST00000509732.6:c.3016C>G	ENSP00000426541.2:p.His1006Asp
ENST00000512211.7:c.3016C>G	ENSP00000423828.3:p.His1006Asp
ENST00000257430.9:c.3016C>G MANE Select	ENSP00000257430.4:p.His1006Asp
ENST00000257430.8:c.3016C>G	ENSP00000257430.4:p.His1006Asp
ENST00000502371.2:c.1369C>G
ENST00000507379.5:c.2962C>G	ENSP00000423224.1:p.His988Asp
ENST00000508376.6:c.3016C>G	ENSP00000427089.2:p.His1006Asp
ENST00000508624.5:c.*2338C>G	ENSP00000424265.1:n.*2338C>G
ENST00000512211.6:c.3016C>G	ENSP00000423828.2:p.His1006Asp
ENST00000520401.1:c.230+9638C>G
NM_000038.5:c.3016C>G	NP_000029.2:p.His1006Asp
NM_001127510.2:c.3016C>G	NP_001120982.1:p.His1006Asp
NM_001127511.2:c.2962C>G	NP_001120983.2:p.His988Asp
NM_001354895.1:c.3016C>G	NP_001341824.1:p.His1006Asp
NM_001354896.1:c.3070C>G	NP_001341825.1:p.His1024Asp
NM_001354897.1:c.3046C>G	NP_001341826.1:p.His1016Asp
NM_001354898.1:c.2941C>G	NP_001341827.1:p.His981Asp
NM_001354899.1:c.2932C>G	NP_001341828.1:p.His978Asp
NM_001354900.1:c.2893C>G	NP_001341829.1:p.His965Asp
NM_001354901.1:c.2839C>G	NP_001341830.1:p.His947Asp
NM_001354902.1:c.2743C>G	NP_001341831.1:p.His915Asp
NM_001354903.1:c.2713C>G	NP_001341832.1:p.His905Asp
NM_001354904.1:c.2638C>G	NP_001341833.1:p.His880Asp
NM_001354905.1:c.2536C>G	NP_001341834.1:p.His846Asp
NM_001354906.1:c.2167C>G	NP_001341835.1:p.His723Asp
NM_000038.6:c.3016C>G MANE Select	NP_000029.2:p.His1006Asp
NM_001127510.3:c.3016C>G	NP_001120982.1:p.His1006Asp
NM_001127511.3:c.2962C>G	NP_001120983.2:p.His988Asp
NM_001354895.2:c.3016C>G	NP_001341824.1:p.His1006Asp
NM_001354896.2:c.3070C>G	NP_001341825.1:p.His1024Asp
NM_001354897.2:c.3046C>G	NP_001341826.1:p.His1016Asp
NM_001354898.2:c.2941C>G	NP_001341827.1:p.His981Asp
NM_001354899.2:c.2932C>G	NP_001341828.1:p.His978Asp
NM_001354900.2:c.2893C>G	NP_001341829.1:p.His965Asp
NM_001354901.2:c.2839C>G	NP_001341830.1:p.His947Asp
NM_001354902.2:c.2743C>G	NP_001341831.1:p.His915Asp
NM_001354903.2:c.2713C>G	NP_001341832.1:p.His905Asp
NM_001354904.2:c.2638C>G	NP_001341833.1:p.His880Asp
NM_001354905.2:c.2536C>G	NP_001341834.1:p.His846Asp
NM_001354906.2:c.2167C>G	NP_001341835.1:p.His723Asp