Canonical Allele Identifier: CA645603173

Gene: ARAF

Linked Data

• COSMIC: COSM5412721

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566727_47566728delinsTT , CM000685.2:g.47566727_47566728delinsTT	GRCh38
NC_000023.10:g.47426126_47426127delinsTT , CM000685.1:g.47426126_47426127delinsTT	GRCh37
NC_000023.9:g.47311070_47311071delinsTT	NCBI36
NG_016339.1:g.10611_10612delinsTT
NG_016339.2:g.10611_10612delinsTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000377045.9:c.646_647delinsTT MANE Select	ENSP00000366244.4:p.Pro216Phe
ENST00000290277.10:c.655_656delinsTT	ENSP00000290277.7:p.Pro219Phe
ENST00000377045.8:c.646_647delinsTT	ENSP00000366244.4:p.Pro216Phe
NM_001256196.1:c.655_656delinsTT	NP_001243125.1:p.Pro219Phe
NM_001654.4:c.646_647delinsTT	NP_001645.1:p.Pro216Phe
XM_006724529.1:c.661_662delinsTT	XP_006724592.1:p.Pro221Phe
XM_011543906.1:c.661_662delinsTT	XP_011542208.1:p.Pro221Phe
XM_011543907.1:c.661_662delinsTT	XP_011542209.1:p.Pro221Phe
XM_011543908.1:c.646_647delinsTT	XP_011542210.1:p.Pro216Phe
XM_011543909.1:c.-12_-11delinsTT	XP_011542211.1:n.-12_-11delinsTT
XM_006724529.3:c.661_662delinsTT	XP_006724592.1:p.Pro221Phe
XM_011543906.3:c.661_662delinsTT	XP_011542208.1:p.Pro221Phe
XM_011543908.3:c.646_647delinsTT	XP_011542210.1:p.Pro216Phe
XM_011543909.3:c.-12_-11delinsTT	XP_011542211.1:n.-12_-11delinsTT
NM_001654.5:c.646_647delinsTT MANE Select	NP_001645.1:p.Pro216Phe
NM_001256196.2:c.655_656delinsTT	NP_001243125.1:p.Pro219Phe