Canonical Allele Identifier: CA2978266
Community Standard Title: NM_025074.7(FRAS1):c.8010C>T (p.Thr2670=)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78477973C>T , CM000666.2:g.78477973C>T GRCh38
NC_000004.11:g.79399127C>T , CM000666.1:g.79399127C>T GRCh37
NC_000004.10:g.79618151C>T NCBI36
NG_015812.1:g.425404C>T
NG_015812.2:g.425404C>T

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.8010C>T MANE Select NP_079350.5:p.Thr2670=
ENST00000512123.4:c.8010C>T MANE Select ENSP00000422834.2:p.Thr2670=
NM_025074.6:c.8010C>T NP_079350.5:p.Thr2670=
ENST00000512123.3:c.8010C>T ENSP00000422834.2:p.Thr2670=
ENST00000682513.1:c.8010C>T ENSP00000508201.1:p.Thr2670=
XM_006714314.1:c.8004C>T XP_006714377.1:p.Thr2668=
XM_006714316.1:c.7782C>T XP_006714379.1:p.Thr2594=
XM_006714316.3:c.7782C>T XP_006714379.1:p.Thr2594=
XM_011532270.1:c.5709C>T XP_011530572.1:p.Thr1903=
XM_011532271.1:c.2898C>T XP_011530573.1:p.Thr966=