Canonical Allele Identifier: CA412813408

Gene: ARAF

Linked Data

• MyVariant Identifiers: chrX:g.47426129A>T (hg19) ; chrX:g.47566730A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566730A>T , CM000685.2:g.47566730A>T	GRCh38
NC_000023.10:g.47426129A>T , CM000685.1:g.47426129A>T	GRCh37
NC_000023.9:g.47311073A>T	NCBI36
NG_016339.1:g.10614A>T
NG_016339.2:g.10614A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377045.9:c.649A>T MANE Select	ENSP00000366244.4:p.Asn217Tyr
ENST00000290277.10:c.658A>T	ENSP00000290277.7:p.Asn220Tyr
ENST00000377045.8:c.649A>T	ENSP00000366244.4:p.Asn217Tyr
NM_001256196.1:c.658A>T	NP_001243125.1:p.Asn220Tyr
NM_001654.4:c.649A>T	NP_001645.1:p.Asn217Tyr
XM_006724529.1:c.664A>T	XP_006724592.1:p.Asn222Tyr
XM_011543906.1:c.664A>T	XP_011542208.1:p.Asn222Tyr
XM_011543907.1:c.664A>T	XP_011542209.1:p.Asn222Tyr
XM_011543908.1:c.649A>T	XP_011542210.1:p.Asn217Tyr
XM_011543909.1:c.-9A>T	XP_011542211.1:n.-9A>T
XM_006724529.3:c.664A>T	XP_006724592.1:p.Asn222Tyr
XM_011543906.3:c.664A>T	XP_011542208.1:p.Asn222Tyr
XM_011543908.3:c.649A>T	XP_011542210.1:p.Asn217Tyr
XM_011543909.3:c.-9A>T	XP_011542211.1:n.-9A>T
NM_001654.5:c.649A>T MANE Select	NP_001645.1:p.Asn217Tyr
NM_001256196.2:c.658A>T	NP_001243125.1:p.Asn220Tyr