Canonical Allele Identifier: CA412813474

Gene: ARAF

Linked Data

• MyVariant Identifiers: chrX:g.47426150A>G (hg19) ; chrX:g.47566751A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566751A>G , CM000685.2:g.47566751A>G	GRCh38
NC_000023.10:g.47426150A>G , CM000685.1:g.47426150A>G	GRCh37
NC_000023.9:g.47311094A>G	NCBI36
NG_016339.1:g.10635A>G
NG_016339.2:g.10635A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377045.9:c.670A>G MANE Select	ENSP00000366244.4:p.Thr224Ala
ENST00000290277.10:c.679A>G	ENSP00000290277.7:p.Thr227Ala
ENST00000377045.8:c.670A>G	ENSP00000366244.4:p.Thr224Ala
NM_001256196.1:c.679A>G	NP_001243125.1:p.Thr227Ala
NM_001654.4:c.670A>G	NP_001645.1:p.Thr224Ala
XM_006724529.1:c.685A>G	XP_006724592.1:p.Thr229Ala
XM_011543906.1:c.685A>G	XP_011542208.1:p.Thr229Ala
XM_011543907.1:c.685A>G	XP_011542209.1:p.Thr229Ala
XM_011543908.1:c.670A>G	XP_011542210.1:p.Thr224Ala
XM_011543909.1:c.13A>G	XP_011542211.1:p.Thr5Ala
XM_006724529.3:c.685A>G	XP_006724592.1:p.Thr229Ala
XM_011543906.3:c.685A>G	XP_011542208.1:p.Thr229Ala
XM_011543908.3:c.670A>G	XP_011542210.1:p.Thr224Ala
XM_011543909.3:c.13A>G	XP_011542211.1:p.Thr5Ala
NM_001654.5:c.670A>G MANE Select	NP_001645.1:p.Thr224Ala
NM_001256196.2:c.679A>G	NP_001243125.1:p.Thr227Ala