Canonical Allele Identifier: CA412813500

Gene: ARAF

Linked Data

• MyVariant Identifiers: chrX:g.47426157C>G (hg19) ; chrX:g.47566758C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566758C>G , CM000685.2:g.47566758C>G	GRCh38
NC_000023.10:g.47426157C>G , CM000685.1:g.47426157C>G	GRCh37
NC_000023.9:g.47311101C>G	NCBI36
NG_016339.1:g.10642C>G
NG_016339.2:g.10642C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377045.9:c.677C>G MANE Select	ENSP00000366244.4:p.Pro226Arg
ENST00000290277.10:c.686C>G	ENSP00000290277.7:p.Pro229Arg
ENST00000377045.8:c.677C>G	ENSP00000366244.4:p.Pro226Arg
NM_001256196.1:c.686C>G	NP_001243125.1:p.Pro229Arg
NM_001654.4:c.677C>G	NP_001645.1:p.Pro226Arg
XM_006724529.1:c.692C>G	XP_006724592.1:p.Pro231Arg
XM_011543906.1:c.692C>G	XP_011542208.1:p.Pro231Arg
XM_011543907.1:c.692C>G	XP_011542209.1:p.Pro231Arg
XM_011543908.1:c.677C>G	XP_011542210.1:p.Pro226Arg
XM_011543909.1:c.20C>G	XP_011542211.1:p.Pro7Arg
XM_006724529.3:c.692C>G	XP_006724592.1:p.Pro231Arg
XM_011543906.3:c.692C>G	XP_011542208.1:p.Pro231Arg
XM_011543908.3:c.677C>G	XP_011542210.1:p.Pro226Arg
XM_011543909.3:c.20C>G	XP_011542211.1:p.Pro7Arg
NM_001654.5:c.677C>G MANE Select	NP_001645.1:p.Pro226Arg
NM_001256196.2:c.686C>G	NP_001243125.1:p.Pro229Arg