Canonical Allele Identifier: CA2427968727
Gene: ARAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47566713_47566728delinsGCTCCACGTCCACTCC , CM000685.2:g.47566713_47566728delinsGCTCCACGTCCACTCC GRCh38
NC_000023.10:g.47426112_47426127delinsGCTCCACGTCCACTCC , CM000685.1:g.47426112_47426127delinsGCTCCACGTCCACTCC GRCh37
NC_000023.9:g.47311056_47311071delinsGCTCCACGTCCACTCC NCBI36
NG_016339.1:g.10597_10612delinsGCTCCACGTCCACTCC
NG_016339.2:g.10597_10612delinsGCTCCACGTCCACTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000377045.9:c.632_647delinsGCTCCACGTCCACTCC MANE Select ENSP00000366244.4:p.Arg211=
ENST00000290277.10:c.641_656delinsGCTCCACGTCCACTCC ENSP00000290277.7:p.Arg214=
ENST00000377045.8:c.632_647delinsGCTCCACGTCCACTCC ENSP00000366244.4:p.Arg211=
NM_001256196.1:c.641_656delinsGCTCCACGTCCACTCC NP_001243125.1:p.Arg214=
NM_001654.4:c.632_647delinsGCTCCACGTCCACTCC NP_001645.1:p.Arg211=
XM_006724529.1:c.647_662delinsGCTCCACGTCCACTCC XP_006724592.1:p.Arg216=
XM_011543906.1:c.647_662delinsGCTCCACGTCCACTCC XP_011542208.1:p.Arg216=
XM_011543907.1:c.647_662delinsGCTCCACGTCCACTCC XP_011542209.1:p.Arg216=
XM_011543908.1:c.632_647delinsGCTCCACGTCCACTCC XP_011542210.1:p.Arg211=
XM_011543909.1:c.-26_-11delinsGCTCCACGTCCACTCC XP_011542211.1:n.-26_-11delinsGCTCCACGTCCACTCC
XM_006724529.3:c.647_662delinsGCTCCACGTCCACTCC XP_006724592.1:p.Arg216=
XM_011543906.3:c.647_662delinsGCTCCACGTCCACTCC XP_011542208.1:p.Arg216=
XM_011543908.3:c.632_647delinsGCTCCACGTCCACTCC XP_011542210.1:p.Arg211=
XM_011543909.3:c.-26_-11delinsGCTCCACGTCCACTCC XP_011542211.1:n.-26_-11delinsGCTCCACGTCCACTCC
NM_001654.5:c.632_647delinsGCTCCACGTCCACTCC MANE Select NP_001645.1:p.Arg211=
NM_001256196.2:c.641_656delinsGCTCCACGTCCACTCC NP_001243125.1:p.Arg214=