Canonical Allele Identifier: CA16042492
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78477962A>G , CM000666.2:g.78477962A>G GRCh38
NC_000004.11:g.79399116A>G , CM000666.1:g.79399116A>G GRCh37
NC_000004.10:g.79618140A>G NCBI36
NG_015812.1:g.425393A>G
NG_015812.2:g.425393A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682513.1:c.7999A>G ENSP00000508201.1:p.Ile2667Val
ENST00000512123.4:c.7999A>G MANE Select ENSP00000422834.2:p.Ile2667Val
ENST00000512123.3:c.7999A>G ENSP00000422834.2:p.Ile2667Val
NM_025074.6:c.7999A>G NP_079350.5:p.Ile2667Val
XM_006714314.1:c.7993A>G XP_006714377.1:p.Ile2665Val
XM_006714316.1:c.7771A>G XP_006714379.1:p.Ile2591Val
XM_011532270.1:c.5698A>G XP_011530572.1:p.Ile1900Val
XM_011532271.1:c.2887A>G XP_011530573.1:p.Ile963Val
XM_006714316.3:c.7771A>G XP_006714379.1:p.Ile2591Val
NM_025074.7:c.7999A>G MANE Select NP_079350.5:p.Ile2667Val