Canonical Allele Identifier: CA2978418
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78481948C>G , CM000666.2:g.78481948C>G GRCh38
NC_000004.11:g.79403102C>G , CM000666.1:g.79403102C>G GRCh37
NC_000004.10:g.79622126C>G NCBI36
NG_015812.1:g.429379C>G
NG_015812.2:g.429379C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682513.1:c.8588C>G ENSP00000508201.1:p.Pro2863Arg
ENST00000512123.4:c.8588C>G MANE Select ENSP00000422834.2:p.Pro2863Arg
ENST00000512123.3:c.8588C>G ENSP00000422834.2:p.Pro2863Arg
NM_025074.6:c.8588C>G NP_079350.5:p.Pro2863Arg
XM_006714314.1:c.8582C>G XP_006714377.1:p.Pro2861Arg
XM_006714316.1:c.8360C>G XP_006714379.1:p.Pro2787Arg
XM_011532270.1:c.6287C>G XP_011530572.1:p.Pro2096Arg
XM_011532271.1:c.3476C>G XP_011530573.1:p.Pro1159Arg
XM_006714316.3:c.8360C>G XP_006714379.1:p.Pro2787Arg
NM_025074.7:c.8588C>G MANE Select NP_079350.5:p.Pro2863Arg