Canonical Allele Identifier: CA2561210337

Gene: ARAF

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566729del , CM000685.2:g.47566729del	GRCh38
NC_000023.10:g.47426128del , CM000685.1:g.47426128del	GRCh37
NC_000023.9:g.47311072del	NCBI36
NG_016339.1:g.10613del
NG_016339.2:g.10613del

Transcript Alleles

HGVS	Amino-acid change
ENST00000377045.9:c.648del MANE Select	ENSP00000366244.4:p.Asn217ThrfsTer?
ENST00000290277.10:c.657del	ENSP00000290277.7:p.Asn220ThrfsTer?
ENST00000377045.8:c.648del	ENSP00000366244.4:p.Asn217ThrfsTer?
NM_001256196.1:c.657del	NP_001243125.1:p.Asn220ThrfsTer?
NM_001654.4:c.648del	NP_001645.1:p.Asn217ThrfsTer?
XM_006724529.1:c.663del	XP_006724592.1:p.Asn222ThrfsTer?
XM_011543906.1:c.663del	XP_011542208.1:p.Asn222ThrfsTer?
XM_011543907.1:c.663del	XP_011542209.1:p.Asn222ThrfsTer?
XM_011543908.1:c.648del	XP_011542210.1:p.Asn217ThrfsTer?
XM_011543909.1:c.-10del	XP_011542211.1:n.-10del
XM_006724529.3:c.663del	XP_006724592.1:p.Asn222ThrfsTer?
XM_011543906.3:c.663del	XP_011542208.1:p.Asn222ThrfsTer?
XM_011543908.3:c.648del	XP_011542210.1:p.Asn217ThrfsTer?
XM_011543909.3:c.-10del	XP_011542211.1:n.-10del
NM_001654.5:c.648del MANE Select	NP_001645.1:p.Asn217ThrfsTer?
NM_001256196.2:c.657del	NP_001243125.1:p.Asn220ThrfsTer?