Canonical Allele Identifier: CA412813397

Gene: ARAF

Linked Data

• dbSNP Id: rs2147905617
• MyVariant Identifiers: chrX:g.47426124C>T (hg19) ; chrX:g.47566725C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566725C>T , CM000685.2:g.47566725C>T	GRCh38
NC_000023.10:g.47426124C>T , CM000685.1:g.47426124C>T	GRCh37
NC_000023.9:g.47311068C>T	NCBI36
NG_016339.1:g.10609C>T
NG_016339.2:g.10609C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000377045.9:c.644C>T MANE Select	ENSP00000366244.4:p.Thr215Ile
ENST00000290277.10:c.653C>T	ENSP00000290277.7:p.Thr218Ile
ENST00000377045.8:c.644C>T	ENSP00000366244.4:p.Thr215Ile
NM_001256196.1:c.653C>T	NP_001243125.1:p.Thr218Ile
NM_001654.4:c.644C>T	NP_001645.1:p.Thr215Ile
XM_006724529.1:c.659C>T	XP_006724592.1:p.Thr220Ile
XM_011543906.1:c.659C>T	XP_011542208.1:p.Thr220Ile
XM_011543907.1:c.659C>T	XP_011542209.1:p.Thr220Ile
XM_011543908.1:c.644C>T	XP_011542210.1:p.Thr215Ile
XM_011543909.1:c.-14C>T	XP_011542211.1:n.-14C>T
XM_006724529.3:c.659C>T	XP_006724592.1:p.Thr220Ile
XM_011543906.3:c.659C>T	XP_011542208.1:p.Thr220Ile
XM_011543908.3:c.644C>T	XP_011542210.1:p.Thr215Ile
XM_011543909.3:c.-14C>T	XP_011542211.1:n.-14C>T
NM_001654.5:c.644C>T MANE Select	NP_001645.1:p.Thr215Ile
NM_001256196.2:c.653C>T	NP_001243125.1:p.Thr218Ile