Canonical Allele Identifier: CA2977779
Community Standard Title: NM_025074.7(FRAS1):c.6433C>T (p.Arg2145Ter)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78450309C>T , CM000666.2:g.78450309C>T GRCh38
NC_000004.11:g.79371463C>T , CM000666.1:g.79371463C>T GRCh37
NC_000004.10:g.79590487C>T NCBI36
NG_015812.1:g.397740C>T
NG_015812.2:g.397740C>T

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.6433C>T MANE Select NP_079350.5:p.Arg2145Ter
ENST00000512123.4:c.6433C>T MANE Select ENSP00000422834.2:p.Arg2145Ter
NM_025074.6:c.6433C>T NP_079350.5:p.Arg2145Ter
ENST00000509802.1:n.418C>T
ENST00000512123.3:c.6433C>T ENSP00000422834.2:p.Arg2145Ter
ENST00000682513.1:c.6433C>T ENSP00000508201.1:p.Arg2145Ter
ENST00000684159.1:c.6433C>T ENSP00000506875.1:p.Arg2145Ter
XM_006714314.1:c.6427C>T XP_006714377.1:p.Arg2143Ter
XM_006714316.1:c.6433C>T XP_006714379.1:p.Arg2145Ter
XM_006714316.3:c.6433C>T XP_006714379.1:p.Arg2145Ter
XM_011532270.1:c.4132C>T XP_011530572.1:p.Arg1378Ter
XM_011532271.1:c.1321C>T XP_011530573.1:p.Arg441Ter