Canonical Allele Identifier: CA16037691
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 433676
dbSNP Id: rs1473460192

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112843119C>T , CM000667.2:g.112843119C>T GRCh38
NC_000005.9:g.112178816C>T , CM000667.1:g.112178816C>T GRCh37
NC_000005.8:g.112206715C>T NCBI36
NG_008481.4:g.155599C>T , LRG_130:g.155599C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000504915.3:c.7579C>T ENSP00000473355.2:p.Pro2527Ser
ENST00000505350.2:c.*7531C>T ENSP00000481752.1:n.*7531C>T
ENST00000507379.6:c.7471C>T ENSP00000423224.2:p.Pro2491Ser
ENST00000509732.6:c.7525C>T ENSP00000426541.2:p.Pro2509Ser
ENST00000512211.7:c.7525C>T ENSP00000423828.3:p.Pro2509Ser
ENST00000257430.9:c.7525C>T MANE Select ENSP00000257430.4:p.Pro2509Ser
ENST00000257430.8:c.7525C>T ENSP00000257430.4:p.Pro2509Ser
ENST00000508376.6:c.7525C>T ENSP00000427089.2:p.Pro2509Ser
ENST00000520401.1:c.231-13530C>T
NM_000038.5:c.7525C>T NP_000029.2:p.Pro2509Ser
NM_001127510.2:c.7525C>T NP_001120982.1:p.Pro2509Ser
NM_001127511.2:c.7471C>T NP_001120983.2:p.Pro2491Ser
NM_001354895.1:c.7525C>T NP_001341824.1:p.Pro2509Ser
NM_001354896.1:c.7579C>T NP_001341825.1:p.Pro2527Ser
NM_001354897.1:c.7555C>T NP_001341826.1:p.Pro2519Ser
NM_001354898.1:c.7450C>T NP_001341827.1:p.Pro2484Ser
NM_001354899.1:c.7441C>T NP_001341828.1:p.Pro2481Ser
NM_001354900.1:c.7402C>T NP_001341829.1:p.Pro2468Ser
NM_001354901.1:c.7348C>T NP_001341830.1:p.Pro2450Ser
NM_001354902.1:c.7252C>T NP_001341831.1:p.Pro2418Ser
NM_001354903.1:c.7222C>T NP_001341832.1:p.Pro2408Ser
NM_001354904.1:c.7147C>T NP_001341833.1:p.Pro2383Ser
NM_001354905.1:c.7045C>T NP_001341834.1:p.Pro2349Ser
NM_001354906.1:c.6676C>T NP_001341835.1:p.Pro2226Ser
NM_000038.6:c.7525C>T MANE Select NP_000029.2:p.Pro2509Ser
NM_001127510.3:c.7525C>T NP_001120982.1:p.Pro2509Ser
NM_001127511.3:c.7471C>T NP_001120983.2:p.Pro2491Ser
NM_001354895.2:c.7525C>T NP_001341824.1:p.Pro2509Ser
NM_001354896.2:c.7579C>T NP_001341825.1:p.Pro2527Ser
NM_001354897.2:c.7555C>T NP_001341826.1:p.Pro2519Ser
NM_001354898.2:c.7450C>T NP_001341827.1:p.Pro2484Ser
NM_001354899.2:c.7441C>T NP_001341828.1:p.Pro2481Ser
NM_001354900.2:c.7402C>T NP_001341829.1:p.Pro2468Ser
NM_001354901.2:c.7348C>T NP_001341830.1:p.Pro2450Ser
NM_001354902.2:c.7252C>T NP_001341831.1:p.Pro2418Ser
NM_001354903.2:c.7222C>T NP_001341832.1:p.Pro2408Ser
NM_001354904.2:c.7147C>T NP_001341833.1:p.Pro2383Ser
NM_001354905.2:c.7045C>T NP_001341834.1:p.Pro2349Ser
NM_001354906.2:c.6676C>T NP_001341835.1:p.Pro2226Ser