Canonical Allele Identifier: CA515989184

Gene: ARAF

Linked Data

• MyVariant Identifiers: chrX:g.47426125T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566726T>C , CM000685.2:g.47566726T>C	GRCh38
NC_000023.10:g.47426125T>C , CM000685.1:g.47426125T>C	GRCh37
NC_000023.9:g.47311069T>C	NCBI36
NG_016339.1:g.10610T>C
NG_016339.2:g.10610T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377045.9:c.645T>C MANE Select	ENSP00000366244.4:p.Thr215=
ENST00000290277.10:c.654T>C	ENSP00000290277.7:p.Thr218=
ENST00000377045.8:c.645T>C	ENSP00000366244.4:p.Thr215=
NM_001256196.1:c.654T>C	NP_001243125.1:p.Thr218=
NM_001654.4:c.645T>C	NP_001645.1:p.Thr215=
XM_006724529.1:c.660T>C	XP_006724592.1:p.Thr220=
XM_011543906.1:c.660T>C	XP_011542208.1:p.Thr220=
XM_011543907.1:c.660T>C	XP_011542209.1:p.Thr220=
XM_011543908.1:c.645T>C	XP_011542210.1:p.Thr215=
XM_011543909.1:c.-13T>C	XP_011542211.1:n.-13T>C
XM_006724529.3:c.660T>C	XP_006724592.1:p.Thr220=
XM_011543906.3:c.660T>C	XP_011542208.1:p.Thr220=
XM_011543908.3:c.645T>C	XP_011542210.1:p.Thr215=
XM_011543909.3:c.-13T>C	XP_011542211.1:n.-13T>C
NM_001654.5:c.645T>C MANE Select	NP_001645.1:p.Thr215=
NM_001256196.2:c.654T>C	NP_001243125.1:p.Thr218=