Canonical Allele Identifier: CA515989238

Gene: ARAF

Linked Data

• dbSNP Id: rs764907490
• MyVariant Identifiers: chrX:g.47426152G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566753G>T , CM000685.2:g.47566753G>T	GRCh38
NC_000023.10:g.47426152G>T , CM000685.1:g.47426152G>T	GRCh37
NC_000023.9:g.47311096G>T	NCBI36
NG_016339.1:g.10637G>T
NG_016339.2:g.10637G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377045.9:c.672G>T MANE Select	ENSP00000366244.4:p.Thr224=
ENST00000290277.10:c.681G>T	ENSP00000290277.7:p.Thr227=
ENST00000377045.8:c.672G>T	ENSP00000366244.4:p.Thr224=
NM_001256196.1:c.681G>T	NP_001243125.1:p.Thr227=
NM_001654.4:c.672G>T	NP_001645.1:p.Thr224=
XM_006724529.1:c.687G>T	XP_006724592.1:p.Thr229=
XM_011543906.1:c.687G>T	XP_011542208.1:p.Thr229=
XM_011543907.1:c.687G>T	XP_011542209.1:p.Thr229=
XM_011543908.1:c.672G>T	XP_011542210.1:p.Thr224=
XM_011543909.1:c.15G>T	XP_011542211.1:p.Thr5=
XM_006724529.3:c.687G>T	XP_006724592.1:p.Thr229=
XM_011543906.3:c.687G>T	XP_011542208.1:p.Thr229=
XM_011543908.3:c.672G>T	XP_011542210.1:p.Thr224=
XM_011543909.3:c.15G>T	XP_011542211.1:p.Thr5=
NM_001654.5:c.672G>T MANE Select	NP_001645.1:p.Thr224=
NM_001256196.2:c.681G>T	NP_001243125.1:p.Thr227=