Canonical Allele Identifier: CA2978505
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78488955G>A , CM000666.2:g.78488955G>A GRCh38
NC_000004.11:g.79410109G>A , CM000666.1:g.79410109G>A GRCh37
NC_000004.10:g.79629133G>A NCBI36
NG_015812.1:g.436386G>A
NG_015812.2:g.436386G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682513.1:c.8833G>A ENSP00000508201.1:p.Gly2945Arg
ENST00000512123.4:c.8833G>A MANE Select ENSP00000422834.2:p.Gly2945Arg
ENST00000512123.3:c.8833G>A ENSP00000422834.2:p.Gly2945Arg
NM_025074.6:c.8833G>A NP_079350.5:p.Gly2945Arg
XM_006714314.1:c.8827G>A XP_006714377.1:p.Gly2943Arg
XM_006714316.1:c.8605G>A XP_006714379.1:p.Gly2869Arg
XM_011532270.1:c.6532G>A XP_011530572.1:p.Gly2178Arg
XM_011532271.1:c.3721G>A XP_011530573.1:p.Gly1241Arg
XM_006714316.3:c.8605G>A XP_006714379.1:p.Gly2869Arg
NM_025074.7:c.8833G>A MANE Select NP_079350.5:p.Gly2945Arg