Canonical Allele Identifier: CA2978101
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78472259C>T , CM000666.2:g.78472259C>T GRCh38
NC_000004.11:g.79393413C>T , CM000666.1:g.79393413C>T GRCh37
NC_000004.10:g.79612437C>T NCBI36
NG_015812.1:g.419690C>T
NG_015812.2:g.419690C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682513.1:c.7451C>T ENSP00000508201.1:p.Thr2484Met
ENST00000512123.4:c.7451C>T MANE Select ENSP00000422834.2:p.Thr2484Met
ENST00000512123.3:c.7451C>T ENSP00000422834.2:p.Thr2484Met
NM_025074.6:c.7451C>T NP_079350.5:p.Thr2484Met
XM_006714314.1:c.7445C>T XP_006714377.1:p.Thr2482Met
XM_006714316.1:c.7223C>T XP_006714379.1:p.Thr2408Met
XM_011532270.1:c.5150C>T XP_011530572.1:p.Thr1717Met
XM_011532271.1:c.2339C>T XP_011530573.1:p.Thr780Met
XM_006714316.3:c.7223C>T XP_006714379.1:p.Thr2408Met
NM_025074.7:c.7451C>T MANE Select NP_079350.5:p.Thr2484Met