Canonical Allele Identifier: CA412813402

Gene: ARAF

Linked Data

• MyVariant Identifiers: chrX:g.47426126C>T (hg19) ; chrX:g.47566727C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566727C>T , CM000685.2:g.47566727C>T	GRCh38
NC_000023.10:g.47426126C>T , CM000685.1:g.47426126C>T	GRCh37
NC_000023.9:g.47311070C>T	NCBI36
NG_016339.1:g.10611C>T
NG_016339.2:g.10611C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000377045.9:c.646C>T MANE Select	ENSP00000366244.4:p.Pro216Ser
ENST00000290277.10:c.655C>T	ENSP00000290277.7:p.Pro219Ser
ENST00000377045.8:c.646C>T	ENSP00000366244.4:p.Pro216Ser
NM_001256196.1:c.655C>T	NP_001243125.1:p.Pro219Ser
NM_001654.4:c.646C>T	NP_001645.1:p.Pro216Ser
XM_006724529.1:c.661C>T	XP_006724592.1:p.Pro221Ser
XM_011543906.1:c.661C>T	XP_011542208.1:p.Pro221Ser
XM_011543907.1:c.661C>T	XP_011542209.1:p.Pro221Ser
XM_011543908.1:c.646C>T	XP_011542210.1:p.Pro216Ser
XM_011543909.1:c.-12C>T	XP_011542211.1:n.-12C>T
XM_006724529.3:c.661C>T	XP_006724592.1:p.Pro221Ser
XM_011543906.3:c.661C>T	XP_011542208.1:p.Pro221Ser
XM_011543908.3:c.646C>T	XP_011542210.1:p.Pro216Ser
XM_011543909.3:c.-12C>T	XP_011542211.1:n.-12C>T
NM_001654.5:c.646C>T MANE Select	NP_001645.1:p.Pro216Ser
NM_001256196.2:c.655C>T	NP_001243125.1:p.Pro219Ser