Canonical Allele Identifier: CA16029705
Community Standard Title: NM_000038.6(APC):c.3817A>T (p.Arg1273Ter)
Gene: APC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112839411A>T , CM000667.2:g.112839411A>T GRCh38
NC_000005.9:g.112175108A>T , CM000667.1:g.112175108A>T GRCh37
NC_000005.8:g.112203007A>T NCBI36
NG_008481.4:g.151891A>T , LRG_130:g.151891A>T

Transcript Alleles

HGVS Amino-acid Change
NM_000038.6:c.3817A>T MANE Select NP_000029.2:p.Arg1273Ter
ENST00000257430.9:c.3817A>T MANE Select ENSP00000257430.4:p.Arg1273Ter
NM_000038.5:c.3817A>T NP_000029.2:p.Arg1273Ter
NM_001127510.2:c.3817A>T NP_001120982.1:p.Arg1273Ter
NM_001127510.3:c.3817A>T NP_001120982.1:p.Arg1273Ter
NM_001127511.2:c.3763A>T NP_001120983.2:p.Arg1255Ter
NM_001127511.3:c.3763A>T NP_001120983.2:p.Arg1255Ter
NM_001354895.1:c.3817A>T NP_001341824.1:p.Arg1273Ter
NM_001354895.2:c.3817A>T NP_001341824.1:p.Arg1273Ter
NM_001354896.1:c.3871A>T NP_001341825.1:p.Arg1291Ter
NM_001354896.2:c.3871A>T NP_001341825.1:p.Arg1291Ter
NM_001354897.1:c.3847A>T NP_001341826.1:p.Arg1283Ter
NM_001354897.2:c.3847A>T NP_001341826.1:p.Arg1283Ter
NM_001354898.1:c.3742A>T NP_001341827.1:p.Arg1248Ter
NM_001354898.2:c.3742A>T NP_001341827.1:p.Arg1248Ter
NM_001354899.1:c.3733A>T NP_001341828.1:p.Arg1245Ter
NM_001354899.2:c.3733A>T NP_001341828.1:p.Arg1245Ter
NM_001354900.1:c.3694A>T NP_001341829.1:p.Arg1232Ter
NM_001354900.2:c.3694A>T NP_001341829.1:p.Arg1232Ter
NM_001354901.1:c.3640A>T NP_001341830.1:p.Arg1214Ter
NM_001354901.2:c.3640A>T NP_001341830.1:p.Arg1214Ter
NM_001354902.1:c.3544A>T NP_001341831.1:p.Arg1182Ter
NM_001354902.2:c.3544A>T NP_001341831.1:p.Arg1182Ter
NM_001354903.1:c.3514A>T NP_001341832.1:p.Arg1172Ter
NM_001354903.2:c.3514A>T NP_001341832.1:p.Arg1172Ter
NM_001354904.1:c.3439A>T NP_001341833.1:p.Arg1147Ter
NM_001354904.2:c.3439A>T NP_001341833.1:p.Arg1147Ter
NM_001354905.1:c.3337A>T NP_001341834.1:p.Arg1113Ter
NM_001354905.2:c.3337A>T NP_001341834.1:p.Arg1113Ter
NM_001354906.1:c.2968A>T NP_001341835.1:p.Arg990Ter
NM_001354906.2:c.2968A>T NP_001341835.1:p.Arg990Ter
ENST00000257430.8:c.3817A>T ENSP00000257430.4:p.Arg1273Ter
ENST00000502371.2:c.2170A>T
ENST00000502371.3:c.3482A>T ENSP00000484935.2:n.3482A>T
ENST00000504915.3:c.3871A>T ENSP00000473355.2:p.Arg1291Ter
ENST00000505350.2:c.*3823A>T ENSP00000481752.1:n.*3823A>T
ENST00000507379.6:c.3763A>T ENSP00000423224.2:p.Arg1255Ter
ENST00000508376.6:c.3817A>T ENSP00000427089.2:p.Arg1273Ter
ENST00000508624.5:c.*3139A>T ENSP00000424265.1:n.*3139A>T
ENST00000509732.6:c.3817A>T ENSP00000426541.2:p.Arg1273Ter
ENST00000512211.6:c.3817A>T ENSP00000423828.2:p.Arg1273Ter
ENST00000512211.7:c.3817A>T ENSP00000423828.3:p.Arg1273Ter
ENST00000520401.1:c.230+10439A>T