Canonical Allele Identifier: CA1470514510
Community Standard Title: NM_025074.7(FRAS1):c.8602C= (p.Gln2868=)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78481962C= , CM000666.2:g.78481962C= GRCh38
NC_000004.11:g.79403116C= , CM000666.1:g.79403116C= GRCh37
NC_000004.10:g.79622140C= NCBI36
NG_015812.1:g.429393C=
NG_015812.2:g.429393C=

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.8602C= MANE Select NP_079350.5:p.Gln2868=
ENST00000512123.4:c.8602C= MANE Select ENSP00000422834.2:p.Gln2868=
NM_025074.6:c.8602C= NP_079350.5:p.Gln2868=
ENST00000512123.3:c.8602C= ENSP00000422834.2:p.Gln2868=
ENST00000682513.1:c.8602C= ENSP00000508201.1:p.Gln2868=
XM_006714314.1:c.8596C= XP_006714377.1:p.Gln2866=
XM_006714316.1:c.8374C= XP_006714379.1:p.Gln2792=
XM_006714316.3:c.8374C= XP_006714379.1:p.Gln2792=
XM_011532270.1:c.6301C= XP_011530572.1:p.Gln2101=
XM_011532271.1:c.3490C= XP_011530573.1:p.Gln1164=