Canonical Allele Identifier: CA412818377
Community Standard Title: NM_001654.5(ARAF):c.1468T>A (p.Ser490Thr)
Gene: ARAF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47569941T>A , CM000685.2:g.47569941T>A GRCh38
NC_000023.10:g.47429340T>A , CM000685.1:g.47429340T>A GRCh37
NC_000023.9:g.47314284T>A NCBI36
NG_008437.1:g.54917A>T
NG_016339.1:g.13825T>A
NG_016339.2:g.13825T>A

Transcript Alleles

HGVS Amino-acid Change
NM_001654.5:c.1468T>A MANE Select NP_001645.1:p.Ser490Thr
ENST00000377045.9:c.1468T>A MANE Select ENSP00000366244.4:p.Ser490Thr
NM_001256196.1:c.1477T>A NP_001243125.1:p.Ser493Thr
NM_001256196.2:c.1477T>A NP_001243125.1:p.Ser493Thr
NM_001654.4:c.1468T>A NP_001645.1:p.Ser490Thr
ENST00000290277.10:c.1477T>A ENSP00000290277.7:p.Ser493Thr
ENST00000377045.8:c.1468T>A ENSP00000366244.4:p.Ser490Thr
ENST00000469505.1:n.248T>A
XM_006724529.1:c.1483T>A XP_006724592.1:p.Ser495Thr
XM_006724529.3:c.1483T>A XP_006724592.1:p.Ser495Thr
XM_011543906.1:c.1483T>A XP_011542208.1:p.Ser495Thr
XM_011543906.3:c.1483T>A XP_011542208.1:p.Ser495Thr
XM_011543907.1:c.1483T>A XP_011542209.1:p.Ser495Thr
XM_011543908.1:c.1468T>A XP_011542210.1:p.Ser490Thr
XM_011543908.3:c.1468T>A XP_011542210.1:p.Ser490Thr
XM_011543909.1:c.811T>A XP_011542211.1:p.Ser271Thr
XM_011543909.3:c.811T>A XP_011542211.1:p.Ser271Thr
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