Canonical Allele Identifier: CA2978663
Community Standard Title: NM_025074.7(FRAS1):c.9446C>T (p.Thr3149Met)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78507550C>T , CM000666.2:g.78507550C>T GRCh38
NC_000004.11:g.79428704C>T , CM000666.1:g.79428704C>T GRCh37
NC_000004.10:g.79647728C>T NCBI36
NG_015812.1:g.454981C>T
NG_015812.2:g.454981C>T

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.9446C>T MANE Select NP_079350.5:p.Thr3149Met
ENST00000512123.4:c.9446C>T MANE Select ENSP00000422834.2:p.Thr3149Met
NM_025074.6:c.9446C>T NP_079350.5:p.Thr3149Met
ENST00000512123.3:c.9446C>T ENSP00000422834.2:p.Thr3149Met
ENST00000682513.1:c.9446C>T ENSP00000508201.1:p.Thr3149Met
XM_006714314.1:c.9440C>T XP_006714377.1:p.Thr3147Met
XM_006714316.1:c.9218C>T XP_006714379.1:p.Thr3073Met
XM_006714316.3:c.9218C>T XP_006714379.1:p.Thr3073Met
XM_011532270.1:c.7145C>T XP_011530572.1:p.Thr2382Met
XM_011532271.1:c.4334C>T XP_011530573.1:p.Thr1445Met