Canonical Allele Identifier: CA412813410

Gene: ARAF

Linked Data

• ClinVar Variation Id: 2496248
• ClinVar RCV Id: RCV003220851
• gnomAD v4: X-47566731-A-G
• MyVariant Identifiers: chrX:g.47426130A>G (hg19) ; chrX:g.47566731A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566731A>G , CM000685.2:g.47566731A>G	GRCh38
NC_000023.10:g.47426130A>G , CM000685.1:g.47426130A>G	GRCh37
NC_000023.9:g.47311074A>G	NCBI36
NG_016339.1:g.10615A>G
NG_016339.2:g.10615A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000377045.9:c.650A>G MANE Select	ENSP00000366244.4:p.Asn217Ser
ENST00000290277.10:c.659A>G	ENSP00000290277.7:p.Asn220Ser
ENST00000377045.8:c.650A>G	ENSP00000366244.4:p.Asn217Ser
NM_001256196.1:c.659A>G	NP_001243125.1:p.Asn220Ser
NM_001654.4:c.650A>G	NP_001645.1:p.Asn217Ser
XM_006724529.1:c.665A>G	XP_006724592.1:p.Asn222Ser
XM_011543906.1:c.665A>G	XP_011542208.1:p.Asn222Ser
XM_011543907.1:c.665A>G	XP_011542209.1:p.Asn222Ser
XM_011543908.1:c.650A>G	XP_011542210.1:p.Asn217Ser
XM_011543909.1:c.-8A>G	XP_011542211.1:n.-8A>G
XM_006724529.3:c.665A>G	XP_006724592.1:p.Asn222Ser
XM_011543906.3:c.665A>G	XP_011542208.1:p.Asn222Ser
XM_011543908.3:c.650A>G	XP_011542210.1:p.Asn217Ser
XM_011543909.3:c.-8A>G	XP_011542211.1:n.-8A>G
NM_001654.5:c.650A>G MANE Select	NP_001645.1:p.Asn217Ser
NM_001256196.2:c.659A>G	NP_001243125.1:p.Asn220Ser