Canonical Allele Identifier: CA16038005

Gene: APC

Linked Data

• dbSNP Id: rs2149991767
• MyVariant Identifiers: chr5:g.112178967C>G (hg19) ; chr5:g.112843270C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112843270C>G , CM000667.2:g.112843270C>G	GRCh38
NC_000005.9:g.112178967C>G , CM000667.1:g.112178967C>G	GRCh37
NC_000005.8:g.112206866C>G	NCBI36
NG_008481.4:g.155750C>G , LRG_130:g.155750C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504915.3:c.7730C>G	ENSP00000473355.2:p.Pro2577Arg
ENST00000505350.2:c.*7682C>G	ENSP00000481752.1:n.*7682C>G
ENST00000507379.6:c.7622C>G	ENSP00000423224.2:p.Pro2541Arg
ENST00000509732.6:c.7676C>G	ENSP00000426541.2:p.Pro2559Arg
ENST00000512211.7:c.7676C>G	ENSP00000423828.3:p.Pro2559Arg
ENST00000257430.9:c.7676C>G MANE Select	ENSP00000257430.4:p.Pro2559Arg
ENST00000257430.8:c.7676C>G	ENSP00000257430.4:p.Pro2559Arg
ENST00000508376.6:c.7676C>G	ENSP00000427089.2:p.Pro2559Arg
ENST00000520401.1:c.231-13379C>G
NM_000038.5:c.7676C>G	NP_000029.2:p.Pro2559Arg
NM_001127510.2:c.7676C>G	NP_001120982.1:p.Pro2559Arg
NM_001127511.2:c.7622C>G	NP_001120983.2:p.Pro2541Arg
NM_001354895.1:c.7676C>G	NP_001341824.1:p.Pro2559Arg
NM_001354896.1:c.7730C>G	NP_001341825.1:p.Pro2577Arg
NM_001354897.1:c.7706C>G	NP_001341826.1:p.Pro2569Arg
NM_001354898.1:c.7601C>G	NP_001341827.1:p.Pro2534Arg
NM_001354899.1:c.7592C>G	NP_001341828.1:p.Pro2531Arg
NM_001354900.1:c.7553C>G	NP_001341829.1:p.Pro2518Arg
NM_001354901.1:c.7499C>G	NP_001341830.1:p.Pro2500Arg
NM_001354902.1:c.7403C>G	NP_001341831.1:p.Pro2468Arg
NM_001354903.1:c.7373C>G	NP_001341832.1:p.Pro2458Arg
NM_001354904.1:c.7298C>G	NP_001341833.1:p.Pro2433Arg
NM_001354905.1:c.7196C>G	NP_001341834.1:p.Pro2399Arg
NM_001354906.1:c.6827C>G	NP_001341835.1:p.Pro2276Arg
NM_000038.6:c.7676C>G MANE Select	NP_000029.2:p.Pro2559Arg
NM_001127510.3:c.7676C>G	NP_001120982.1:p.Pro2559Arg
NM_001127511.3:c.7622C>G	NP_001120983.2:p.Pro2541Arg
NM_001354895.2:c.7676C>G	NP_001341824.1:p.Pro2559Arg
NM_001354896.2:c.7730C>G	NP_001341825.1:p.Pro2577Arg
NM_001354897.2:c.7706C>G	NP_001341826.1:p.Pro2569Arg
NM_001354898.2:c.7601C>G	NP_001341827.1:p.Pro2534Arg
NM_001354899.2:c.7592C>G	NP_001341828.1:p.Pro2531Arg
NM_001354900.2:c.7553C>G	NP_001341829.1:p.Pro2518Arg
NM_001354901.2:c.7499C>G	NP_001341830.1:p.Pro2500Arg
NM_001354902.2:c.7403C>G	NP_001341831.1:p.Pro2468Arg
NM_001354903.2:c.7373C>G	NP_001341832.1:p.Pro2458Arg
NM_001354904.2:c.7298C>G	NP_001341833.1:p.Pro2433Arg
NM_001354905.2:c.7196C>G	NP_001341834.1:p.Pro2399Arg
NM_001354906.2:c.6827C>G	NP_001341835.1:p.Pro2276Arg