Canonical Allele Identifier: CA412813393

Gene: ARAF

Linked Data

• dbSNP Id: rs1057519786
• COSMIC: COSM5416443
• MyVariant Identifiers: chrX:g.47426121C>A (hg19) ; chrX:g.47566722C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377045.9:c.641C>A MANE Select	ENSP00000366244.4:p.Ser214Tyr
ENST00000290277.10:c.650C>A	ENSP00000290277.7:p.Ser217Tyr
ENST00000377045.8:c.641C>A	ENSP00000366244.4:p.Ser214Tyr
NM_001256196.1:c.650C>A	NP_001243125.1:p.Ser217Tyr
NM_001654.4:c.641C>A	NP_001645.1:p.Ser214Tyr
XM_006724529.1:c.656C>A	XP_006724592.1:p.Ser219Tyr
XM_011543906.1:c.656C>A	XP_011542208.1:p.Ser219Tyr
XM_011543907.1:c.656C>A	XP_011542209.1:p.Ser219Tyr
XM_011543908.1:c.641C>A	XP_011542210.1:p.Ser214Tyr
XM_011543909.1:c.-17C>A	XP_011542211.1:n.-17C>A
XM_006724529.3:c.656C>A	XP_006724592.1:p.Ser219Tyr
XM_011543906.3:c.656C>A	XP_011542208.1:p.Ser219Tyr
XM_011543908.3:c.641C>A	XP_011542210.1:p.Ser214Tyr
XM_011543909.3:c.-17C>A	XP_011542211.1:n.-17C>A
NM_001654.5:c.641C>A MANE Select	NP_001645.1:p.Ser214Tyr
NM_001256196.2:c.650C>A	NP_001243125.1:p.Ser217Tyr