Canonical Allele Identifier: CA2978628
Community Standard Title: NM_025074.7(FRAS1):c.9296G>A (p.Arg3099Gln)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78499901G>A , CM000666.2:g.78499901G>A GRCh38
NC_000004.11:g.79421055G>A , CM000666.1:g.79421055G>A GRCh37
NC_000004.10:g.79640079G>A NCBI36
NG_015812.1:g.447332G>A
NG_015812.2:g.447332G>A

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.9296G>A MANE Select NP_079350.5:p.Arg3099Gln
ENST00000512123.4:c.9296G>A MANE Select ENSP00000422834.2:p.Arg3099Gln
NM_025074.6:c.9296G>A NP_079350.5:p.Arg3099Gln
ENST00000512123.3:c.9296G>A ENSP00000422834.2:p.Arg3099Gln
ENST00000682513.1:c.9296G>A ENSP00000508201.1:p.Arg3099Gln
XM_006714314.1:c.9290G>A XP_006714377.1:p.Arg3097Gln
XM_006714316.1:c.9068G>A XP_006714379.1:p.Arg3023Gln
XM_006714316.3:c.9068G>A XP_006714379.1:p.Arg3023Gln
XM_011532270.1:c.6995G>A XP_011530572.1:p.Arg2332Gln
XM_011532271.1:c.4184G>A XP_011530573.1:p.Arg1395Gln