Canonical Allele Identifier: CA357380458
Community Standard Title: NM_025074.7(FRAS1):c.9627C>A (p.Tyr3209Ter)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78508853C>A , CM000666.2:g.78508853C>A GRCh38
NC_000004.11:g.79430007C>A , CM000666.1:g.79430007C>A GRCh37
NC_000004.10:g.79649031C>A NCBI36
NG_015812.1:g.456284C>A
NG_015812.2:g.456284C>A

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.9627C>A MANE Select NP_079350.5:p.Tyr3209Ter
ENST00000512123.4:c.9627C>A MANE Select ENSP00000422834.2:p.Tyr3209Ter
NM_025074.6:c.9627C>A NP_079350.5:p.Tyr3209Ter
ENST00000512123.3:c.9627C>A ENSP00000422834.2:p.Tyr3209Ter
ENST00000682513.1:c.9627C>A ENSP00000508201.1:p.Tyr3209Ter
XM_006714314.1:c.9621C>A XP_006714377.1:p.Tyr3207Ter
XM_006714316.1:c.9399C>A XP_006714379.1:p.Tyr3133Ter
XM_006714316.3:c.9399C>A XP_006714379.1:p.Tyr3133Ter
XM_011532270.1:c.7326C>A XP_011530572.1:p.Tyr2442Ter
XM_011532271.1:c.4515C>A XP_011530573.1:p.Tyr1505Ter