Canonical Allele Identifier: CA2979319
Community Standard Title: NM_025074.7(FRAS1):c.11881C>T (p.Arg3961Trp)
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78540966C>T , CM000666.2:g.78540966C>T GRCh38
NC_000004.11:g.79462120C>T , CM000666.1:g.79462120C>T GRCh37
NC_000004.10:g.79681144C>T NCBI36
NG_015812.1:g.488397C>T
NG_015812.2:g.488397C>T

Transcript Alleles

HGVS Amino-acid Change
NM_025074.7:c.11881C>T MANE Select NP_079350.5:p.Arg3961Trp
ENST00000512123.4:c.11881C>T MANE Select ENSP00000422834.2:p.Arg3961Trp
NM_025074.6:c.11881C>T NP_079350.5:p.Arg3961Trp
ENST00000512123.3:c.11881C>T ENSP00000422834.2:p.Arg3961Trp
XM_006714314.1:c.11875C>T XP_006714377.1:p.Arg3959Trp
XM_006714316.1:c.11653C>T XP_006714379.1:p.Arg3885Trp
XM_006714316.3:c.11653C>T XP_006714379.1:p.Arg3885Trp
XM_011532270.1:c.9580C>T XP_011530572.1:p.Arg3194Trp
XM_011532271.1:c.6769C>T XP_011530573.1:p.Arg2257Trp