Canonical Allele Identifier: CA2427968731

Gene: ARAF

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566722C= , CM000685.2:g.47566722C=	GRCh38
NC_000023.10:g.47426121C= , CM000685.1:g.47426121C=	GRCh37
NC_000023.9:g.47311065C=	NCBI36
NG_016339.1:g.10606C=
NG_016339.2:g.10606C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377045.9:c.641C= MANE Select	ENSP00000366244.4:p.Ser214=
ENST00000290277.10:c.650C=	ENSP00000290277.7:p.Ser217=
ENST00000377045.8:c.641C=	ENSP00000366244.4:p.Ser214=
NM_001256196.1:c.650C=	NP_001243125.1:p.Ser217=
NM_001654.4:c.641C=	NP_001645.1:p.Ser214=
XM_006724529.1:c.656C=	XP_006724592.1:p.Ser219=
XM_011543906.1:c.656C=	XP_011542208.1:p.Ser219=
XM_011543907.1:c.656C=	XP_011542209.1:p.Ser219=
XM_011543908.1:c.641C=	XP_011542210.1:p.Ser214=
XM_011543909.1:c.-17C=	XP_011542211.1:n.-17C=
XM_006724529.3:c.656C=	XP_006724592.1:p.Ser219=
XM_011543906.3:c.656C=	XP_011542208.1:p.Ser219=
XM_011543908.3:c.641C=	XP_011542210.1:p.Ser214=
XM_011543909.3:c.-17C=	XP_011542211.1:n.-17C=
NM_001654.5:c.641C= MANE Select	NP_001645.1:p.Ser214=
NM_001256196.2:c.650C=	NP_001243125.1:p.Ser217=