Canonical Allele Identifier: CA412813532

Gene: ARAF

Linked Data

• MyVariant Identifiers: chrX:g.47426165T>A (hg19) ; chrX:g.47566766T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566766T>A , CM000685.2:g.47566766T>A	GRCh38
NC_000023.10:g.47426165T>A , CM000685.1:g.47426165T>A	GRCh37
NC_000023.9:g.47311109T>A	NCBI36
NG_016339.1:g.10650T>A
NG_016339.2:g.10650T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377045.9:c.685T>A MANE Select	ENSP00000366244.4:p.Ser229Thr
ENST00000290277.10:c.694T>A	ENSP00000290277.7:p.Ser232Thr
ENST00000377045.8:c.685T>A	ENSP00000366244.4:p.Ser229Thr
NM_001256196.1:c.694T>A	NP_001243125.1:p.Ser232Thr
NM_001654.4:c.685T>A	NP_001645.1:p.Ser229Thr
XM_006724529.1:c.700T>A	XP_006724592.1:p.Ser234Thr
XM_011543906.1:c.700T>A	XP_011542208.1:p.Ser234Thr
XM_011543907.1:c.700T>A	XP_011542209.1:p.Ser234Thr
XM_011543908.1:c.685T>A	XP_011542210.1:p.Ser229Thr
XM_011543909.1:c.28T>A	XP_011542211.1:p.Ser10Thr
XM_006724529.3:c.700T>A	XP_006724592.1:p.Ser234Thr
XM_011543906.3:c.700T>A	XP_011542208.1:p.Ser234Thr
XM_011543908.3:c.685T>A	XP_011542210.1:p.Ser229Thr
XM_011543909.3:c.28T>A	XP_011542211.1:p.Ser10Thr
NM_001654.5:c.685T>A MANE Select	NP_001645.1:p.Ser229Thr
NM_001256196.2:c.694T>A	NP_001243125.1:p.Ser232Thr