Canonical Allele Identifier: CA2674863782
Gene: APC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112737903G>T , CM000667.2:g.112737903G>T GRCh38
NC_000005.9:g.112073600G>T , CM000667.1:g.112073600G>T GRCh37
NC_000005.8:g.112101499G>T NCBI36
NG_008481.4:g.50383G>T , LRG_130:g.50383G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.-41G>T ENSP00000473355.2:n.-41G>T
ENST00000505084.2:n.16G>T
ENST00000505350.2:c.166-16970G>T ENSP00000481752.1:n.166-16970G>T
ENST00000507379.6:c.166-28423G>T ENSP00000423224.2:n.166-28423G>T
ENST00000509732.6:c.-18-16970G>T ENSP00000426541.2:n.-18-16970G>T
ENST00000257430.9:c.-41G>T MANE Select ENSP00000257430.4:n.-41G>T
ENST00000257430.8:c.-41G>T ENSP00000257430.4:n.-41G>T
ENST00000505350.1:c.166-16970G>T ENSP00000481752.1:n.166-16970G>T
ENST00000507379.5:c.166-28423G>T ENSP00000423224.1:n.166-28423G>T
ENST00000508376.6:c.-149G>T ENSP00000427089.2:n.-149G>T
ENST00000508624.5:c.-41G>T ENSP00000424265.1:n.-41G>T
ENST00000509732.5:c.-18-16970G>T ENSP00000426541.1:n.-18-16970G>T
NM_000038.5:c.-41G>T NP_000029.2:n.-41G>T
NM_001127510.2:c.-149G>T NP_001120982.1:n.-149G>T
NM_001127511.2:c.166-28423G>T NP_001120983.2:n.166-28423G>T
NM_001354895.1:c.-18-16970G>T NP_001341824.1:n.-18-16970G>T
NM_001354896.1:c.-41G>T NP_001341825.1:n.-41G>T
NM_001354897.1:c.166-28423G>T NP_001341826.1:n.166-28423G>T
NM_001354898.1:c.-71G>T NP_001341827.1:n.-71G>T
NM_001354899.1:c.-41G>T NP_001341828.1:n.-41G>T
NM_001354900.1:c.-65G>T NP_001341829.1:n.-65G>T
NM_001354901.1:c.-65G>T NP_001341830.1:n.-65G>T
NM_001354902.1:c.166-28423G>T NP_001341831.1:n.166-28423G>T
NM_001354903.1:c.-41G>T NP_001341832.1:n.-41G>T
NM_001354904.1:c.-71G>T NP_001341833.1:n.-71G>T
NM_001354905.1:c.-65G>T NP_001341834.1:n.-65G>T
NM_001354906.1:c.-1076G>T NP_001341835.1:n.-1076G>T
NM_000038.6:c.-41G>T MANE Select NP_000029.2:n.-41G>T
NM_001127510.3:c.-149G>T NP_001120982.1:n.-149G>T
NM_001127511.3:c.166-28423G>T NP_001120983.2:n.166-28423G>T
NM_001354895.2:c.-18-16970G>T NP_001341824.1:n.-18-16970G>T
NM_001354896.2:c.-41G>T NP_001341825.1:n.-41G>T
NM_001354897.2:c.166-28423G>T NP_001341826.1:n.166-28423G>T
NM_001354898.2:c.-71G>T NP_001341827.1:n.-71G>T
NM_001354899.2:c.-41G>T NP_001341828.1:n.-41G>T
NM_001354900.2:c.-65G>T NP_001341829.1:n.-65G>T
NM_001354901.2:c.-65G>T NP_001341830.1:n.-65G>T
NM_001354902.2:c.166-28423G>T NP_001341831.1:n.166-28423G>T
NM_001354903.2:c.-41G>T NP_001341832.1:n.-41G>T
NM_001354904.2:c.-71G>T NP_001341833.1:n.-71G>T
NM_001354905.2:c.-65G>T NP_001341834.1:n.-65G>T
NM_001354906.2:c.-1076G>T NP_001341835.1:n.-1076G>T