Canonical Allele Identifier: CA2978906
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78515885C>T , CM000666.2:g.78515885C>T GRCh38
NC_000004.11:g.79437039C>T , CM000666.1:g.79437039C>T GRCh37
NC_000004.10:g.79656063C>T NCBI36
NG_015812.1:g.463316C>T
NG_015812.2:g.463316C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000512123.4:c.10261C>T MANE Select ENSP00000422834.2:p.Arg3421Ter
ENST00000512123.3:c.10261C>T ENSP00000422834.2:p.Arg3421Ter
NM_025074.6:c.10261C>T NP_079350.5:p.Arg3421Ter
XM_006714314.1:c.10255C>T XP_006714377.1:p.Arg3419Ter
XM_006714316.1:c.10033C>T XP_006714379.1:p.Arg3345Ter
XM_011532270.1:c.7960C>T XP_011530572.1:p.Arg2654Ter
XM_011532271.1:c.5149C>T XP_011530573.1:p.Arg1717Ter
XM_006714316.3:c.10033C>T XP_006714379.1:p.Arg3345Ter
NM_025074.7:c.10261C>T MANE Select NP_079350.5:p.Arg3421Ter