Canonical Allele Identifier: CA515989177

Gene: ARAF

Linked Data

• gnomAD v4: X-47566723-C-G
• MyVariant Identifiers: chrX:g.47426122C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566723C>G , CM000685.2:g.47566723C>G	GRCh38
NC_000023.10:g.47426122C>G , CM000685.1:g.47426122C>G	GRCh37
NC_000023.9:g.47311066C>G	NCBI36
NG_016339.1:g.10607C>G
NG_016339.2:g.10607C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000377045.9:c.642C>G MANE Select	ENSP00000366244.4:p.Ser214=
ENST00000290277.10:c.651C>G	ENSP00000290277.7:p.Ser217=
ENST00000377045.8:c.642C>G	ENSP00000366244.4:p.Ser214=
NM_001256196.1:c.651C>G	NP_001243125.1:p.Ser217=
NM_001654.4:c.642C>G	NP_001645.1:p.Ser214=
XM_006724529.1:c.657C>G	XP_006724592.1:p.Ser219=
XM_011543906.1:c.657C>G	XP_011542208.1:p.Ser219=
XM_011543907.1:c.657C>G	XP_011542209.1:p.Ser219=
XM_011543908.1:c.642C>G	XP_011542210.1:p.Ser214=
XM_011543909.1:c.-16C>G	XP_011542211.1:n.-16C>G
XM_006724529.3:c.657C>G	XP_006724592.1:p.Ser219=
XM_011543906.3:c.657C>G	XP_011542208.1:p.Ser219=
XM_011543908.3:c.642C>G	XP_011542210.1:p.Ser214=
XM_011543909.3:c.-16C>G	XP_011542211.1:n.-16C>G
NM_001654.5:c.642C>G MANE Select	NP_001645.1:p.Ser214=
NM_001256196.2:c.651C>G	NP_001243125.1:p.Ser217=