Canonical Allele Identifier: CA412813313

Gene: ARAF

Linked Data

• dbSNP Id: rs2147905515
• MyVariant Identifiers: chrX:g.47426081G>C (hg19) ; chrX:g.47566682G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566682G>C , CM000685.2:g.47566682G>C	GRCh38
NC_000023.10:g.47426081G>C , CM000685.1:g.47426081G>C	GRCh37
NC_000023.9:g.47311025G>C	NCBI36
NG_016339.1:g.10566G>C
NG_016339.2:g.10566G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377045.9:c.601G>C MANE Select	ENSP00000366244.4:p.Ala201Pro
ENST00000290277.10:c.610G>C	ENSP00000290277.7:p.Ala204Pro
ENST00000377045.8:c.601G>C	ENSP00000366244.4:p.Ala201Pro
NM_001256196.1:c.610G>C	NP_001243125.1:p.Ala204Pro
NM_001654.4:c.601G>C	NP_001645.1:p.Ala201Pro
XM_006724529.1:c.616G>C	XP_006724592.1:p.Ala206Pro
XM_011543906.1:c.616G>C	XP_011542208.1:p.Ala206Pro
XM_011543907.1:c.616G>C	XP_011542209.1:p.Ala206Pro
XM_011543908.1:c.601G>C	XP_011542210.1:p.Ala201Pro
XM_011543909.1:c.-57G>C	XP_011542211.1:n.-57G>C
XM_006724529.3:c.616G>C	XP_006724592.1:p.Ala206Pro
XM_011543906.3:c.616G>C	XP_011542208.1:p.Ala206Pro
XM_011543908.3:c.601G>C	XP_011542210.1:p.Ala201Pro
XM_011543909.3:c.-57G>C	XP_011542211.1:n.-57G>C
NM_001654.5:c.601G>C MANE Select	NP_001645.1:p.Ala201Pro
NM_001256196.2:c.610G>C	NP_001243125.1:p.Ala204Pro