Canonical Allele Identifier: CA2832580869
Gene: ARAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47566643dup , CM000685.2:g.47566643dup GRCh38
NC_000023.10:g.47426042dup , CM000685.1:g.47426042dup GRCh37
NC_000023.9:g.47310986dup NCBI36
NG_016339.1:g.10527dup
NG_016339.2:g.10527dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000377045.9:c.562dup MANE Select ENSP00000366244.4:p.Arg188ProfsTer6
ENST00000290277.10:c.571dup ENSP00000290277.7:p.Arg191ProfsTer6
ENST00000377045.8:c.562dup ENSP00000366244.4:p.Arg188ProfsTer6
NM_001256196.1:c.571dup NP_001243125.1:p.Arg191ProfsTer6
NM_001654.4:c.562dup NP_001645.1:p.Arg188ProfsTer6
XM_006724529.1:c.577dup XP_006724592.1:p.Arg193ProfsTer6
XM_011543906.1:c.577dup XP_011542208.1:p.Arg193ProfsTer6
XM_011543907.1:c.577dup XP_011542209.1:p.Arg193ProfsTer6
XM_011543908.1:c.562dup XP_011542210.1:p.Arg188ProfsTer6
XM_011543909.1:c.-96dup XP_011542211.1:n.-96dup
XM_006724529.3:c.577dup XP_006724592.1:p.Arg193ProfsTer6
XM_011543906.3:c.577dup XP_011542208.1:p.Arg193ProfsTer6
XM_011543908.3:c.562dup XP_011542210.1:p.Arg188ProfsTer6
XM_011543909.3:c.-96dup XP_011542211.1:n.-96dup
NM_001654.5:c.562dup MANE Select NP_001645.1:p.Arg188ProfsTer6
NM_001256196.2:c.571dup NP_001243125.1:p.Arg191ProfsTer6