Canonical Allele Identifier: CA412813409

Gene: ARAF

Linked Data

• MyVariant Identifiers: chrX:g.47426130A>C (hg19) ; chrX:g.47566731A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000377045.9:c.650A>C MANE Select	ENSP00000366244.4:p.Asn217Thr
ENST00000290277.10:c.659A>C	ENSP00000290277.7:p.Asn220Thr
ENST00000377045.8:c.650A>C	ENSP00000366244.4:p.Asn217Thr
NM_001256196.1:c.659A>C	NP_001243125.1:p.Asn220Thr
NM_001654.4:c.650A>C	NP_001645.1:p.Asn217Thr
XM_006724529.1:c.665A>C	XP_006724592.1:p.Asn222Thr
XM_011543906.1:c.665A>C	XP_011542208.1:p.Asn222Thr
XM_011543907.1:c.665A>C	XP_011542209.1:p.Asn222Thr
XM_011543908.1:c.650A>C	XP_011542210.1:p.Asn217Thr
XM_011543909.1:c.-8A>C	XP_011542211.1:n.-8A>C
XM_006724529.3:c.665A>C	XP_006724592.1:p.Asn222Thr
XM_011543906.3:c.665A>C	XP_011542208.1:p.Asn222Thr
XM_011543908.3:c.650A>C	XP_011542210.1:p.Asn217Thr
XM_011543909.3:c.-8A>C	XP_011542211.1:n.-8A>C
NM_001654.5:c.650A>C MANE Select	NP_001645.1:p.Asn217Thr
NM_001256196.2:c.659A>C	NP_001243125.1:p.Asn220Thr