Canonical Allele Identifier: CA412813386

Gene: ARAF

Linked Data

• MyVariant Identifiers: chrX:g.47426117A>T (hg19) ; chrX:g.47566718A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566718A>T , CM000685.2:g.47566718A>T	GRCh38
NC_000023.10:g.47426117A>T , CM000685.1:g.47426117A>T	GRCh37
NC_000023.9:g.47311061A>T	NCBI36
NG_016339.1:g.10602A>T
NG_016339.2:g.10602A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377045.9:c.637A>T MANE Select	ENSP00000366244.4:p.Thr213Ser
ENST00000290277.10:c.646A>T	ENSP00000290277.7:p.Thr216Ser
ENST00000377045.8:c.637A>T	ENSP00000366244.4:p.Thr213Ser
NM_001256196.1:c.646A>T	NP_001243125.1:p.Thr216Ser
NM_001654.4:c.637A>T	NP_001645.1:p.Thr213Ser
XM_006724529.1:c.652A>T	XP_006724592.1:p.Thr218Ser
XM_011543906.1:c.652A>T	XP_011542208.1:p.Thr218Ser
XM_011543907.1:c.652A>T	XP_011542209.1:p.Thr218Ser
XM_011543908.1:c.637A>T	XP_011542210.1:p.Thr213Ser
XM_011543909.1:c.-21A>T	XP_011542211.1:n.-21A>T
XM_006724529.3:c.652A>T	XP_006724592.1:p.Thr218Ser
XM_011543906.3:c.652A>T	XP_011542208.1:p.Thr218Ser
XM_011543908.3:c.637A>T	XP_011542210.1:p.Thr213Ser
XM_011543909.3:c.-21A>T	XP_011542211.1:n.-21A>T
NM_001654.5:c.637A>T MANE Select	NP_001645.1:p.Thr213Ser
NM_001256196.2:c.646A>T	NP_001243125.1:p.Thr216Ser