Canonical Allele Identifier: CA99950940
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78475596A>T , CM000666.2:g.78475596A>T GRCh38
NC_000004.11:g.79396750A>T , CM000666.1:g.79396750A>T GRCh37
NC_000004.10:g.79615774A>T NCBI36
NG_015812.1:g.423027A>T
NG_015812.2:g.423027A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682513.1:c.7841A>T ENSP00000508201.1:p.Tyr2614Phe
ENST00000512123.4:c.7841A>T MANE Select ENSP00000422834.2:p.Tyr2614Phe
ENST00000512123.3:c.7841A>T ENSP00000422834.2:p.Tyr2614Phe
NM_025074.6:c.7841A>T NP_079350.5:p.Tyr2614Phe
XM_006714314.1:c.7835A>T XP_006714377.1:p.Tyr2612Phe
XM_006714316.1:c.7613A>T XP_006714379.1:p.Tyr2538Phe
XM_011532270.1:c.5540A>T XP_011530572.1:p.Tyr1847Phe
XM_011532271.1:c.2729A>T XP_011530573.1:p.Tyr910Phe
XM_006714316.3:c.7613A>T XP_006714379.1:p.Tyr2538Phe
NM_025074.7:c.7841A>T MANE Select NP_079350.5:p.Tyr2614Phe