Canonical Allele Identifier: CA99984844
Community Standard Title: NM_025074.7(FRAS1):c.7084C>T (p.Arg2362Ter)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78466262C>T , CM000666.2:g.78466262C>T GRCh38
NC_000004.11:g.79387416C>T , CM000666.1:g.79387416C>T GRCh37
NC_000004.10:g.79606440C>T NCBI36
NG_015812.1:g.413693C>T
NG_015812.2:g.413693C>T

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.7084C>T MANE Select NP_079350.5:p.Arg2362Ter
ENST00000512123.4:c.7084C>T MANE Select ENSP00000422834.2:p.Arg2362Ter
NM_025074.6:c.7084C>T NP_079350.5:p.Arg2362Ter
ENST00000512123.3:c.7084C>T ENSP00000422834.2:p.Arg2362Ter
ENST00000682513.1:c.7084C>T ENSP00000508201.1:p.Arg2362Ter
XM_006714314.1:c.7078C>T XP_006714377.1:p.Arg2360Ter
XM_006714316.1:c.7029+1679C>T XP_006714379.1:n.7029+1679C>T
XM_006714316.3:c.7029+1679C>T XP_006714379.1:n.7029+1679C>T
XM_011532270.1:c.4783C>T XP_011530572.1:p.Arg1595Ter
XM_011532271.1:c.1972C>T XP_011530573.1:p.Arg658Ter