Canonical Allele Identifier: CA357379428
Community Standard Title: NM_025074.7(FRAS1):c.9466G>T (p.Glu3156Ter)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78507570G>T , CM000666.2:g.78507570G>T GRCh38
NC_000004.11:g.79428724G>T , CM000666.1:g.79428724G>T GRCh37
NC_000004.10:g.79647748G>T NCBI36
NG_015812.1:g.455001G>T
NG_015812.2:g.455001G>T

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.9466G>T MANE Select NP_079350.5:p.Glu3156Ter
ENST00000512123.4:c.9466G>T MANE Select ENSP00000422834.2:p.Glu3156Ter
NM_025074.6:c.9466G>T NP_079350.5:p.Glu3156Ter
ENST00000512123.3:c.9466G>T ENSP00000422834.2:p.Glu3156Ter
ENST00000682513.1:c.9466G>T ENSP00000508201.1:p.Glu3156Ter
XM_006714314.1:c.9460G>T XP_006714377.1:p.Glu3154Ter
XM_006714316.1:c.9238G>T XP_006714379.1:p.Glu3080Ter
XM_006714316.3:c.9238G>T XP_006714379.1:p.Glu3080Ter
XM_011532270.1:c.7165G>T XP_011530572.1:p.Glu2389Ter
XM_011532271.1:c.4354G>T XP_011530573.1:p.Glu1452Ter