Canonical Allele Identifier: CA99980617
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78526552C>G , CM000666.2:g.78526552C>G GRCh38
NC_000004.11:g.79447706C>G , CM000666.1:g.79447706C>G GRCh37
NC_000004.10:g.79666730C>G NCBI36
NG_015812.1:g.473983C>G
NG_015812.2:g.473983C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000512123.4:c.10820C>G MANE Select ENSP00000422834.2:p.Ser3607Ter
ENST00000512123.3:c.10820C>G ENSP00000422834.2:p.Ser3607Ter
NM_025074.6:c.10820C>G NP_079350.5:p.Ser3607Ter
XM_006714314.1:c.10814C>G XP_006714377.1:p.Ser3605Ter
XM_006714316.1:c.10592C>G XP_006714379.1:p.Ser3531Ter
XM_011532270.1:c.8519C>G XP_011530572.1:p.Ser2840Ter
XM_011532271.1:c.5708C>G XP_011530573.1:p.Ser1903Ter
XM_006714316.3:c.10592C>G XP_006714379.1:p.Ser3531Ter
NM_025074.7:c.10820C>G MANE Select NP_079350.5:p.Ser3607Ter