Canonical Allele Identifier: CA412813391

Gene: ARAF

Linked Data

• dbSNP Id: rs1057519876
• COSMIC: COSM6187401
• MyVariant Identifiers: chrX:g.47426120T>A (hg19) ; chrX:g.47566721T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566721T>A , CM000685.2:g.47566721T>A	GRCh38
NC_000023.10:g.47426120T>A , CM000685.1:g.47426120T>A	GRCh37
NC_000023.9:g.47311064T>A	NCBI36
NG_016339.1:g.10605T>A
NG_016339.2:g.10605T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000377045.9:c.640T>A MANE Select	ENSP00000366244.4:p.Ser214Thr
ENST00000290277.10:c.649T>A	ENSP00000290277.7:p.Ser217Thr
ENST00000377045.8:c.640T>A	ENSP00000366244.4:p.Ser214Thr
NM_001256196.1:c.649T>A	NP_001243125.1:p.Ser217Thr
NM_001654.4:c.640T>A	NP_001645.1:p.Ser214Thr
XM_006724529.1:c.655T>A	XP_006724592.1:p.Ser219Thr
XM_011543906.1:c.655T>A	XP_011542208.1:p.Ser219Thr
XM_011543907.1:c.655T>A	XP_011542209.1:p.Ser219Thr
XM_011543908.1:c.640T>A	XP_011542210.1:p.Ser214Thr
XM_011543909.1:c.-18T>A	XP_011542211.1:n.-18T>A
XM_006724529.3:c.655T>A	XP_006724592.1:p.Ser219Thr
XM_011543906.3:c.655T>A	XP_011542208.1:p.Ser219Thr
XM_011543908.3:c.640T>A	XP_011542210.1:p.Ser214Thr
XM_011543909.3:c.-18T>A	XP_011542211.1:n.-18T>A
NM_001654.5:c.640T>A MANE Select	NP_001645.1:p.Ser214Thr
NM_001256196.2:c.649T>A	NP_001243125.1:p.Ser217Thr