Canonical Allele Identifier: CA2978376
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78481809G>A , CM000666.2:g.78481809G>A GRCh38
NC_000004.11:g.79402963G>A , CM000666.1:g.79402963G>A GRCh37
NC_000004.10:g.79621987G>A NCBI36
NG_015812.1:g.429240G>A
NG_015812.2:g.429240G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682513.1:c.8449G>A ENSP00000508201.1:p.Val2817Ile
ENST00000512123.4:c.8449G>A MANE Select ENSP00000422834.2:p.Val2817Ile
ENST00000512123.3:c.8449G>A ENSP00000422834.2:p.Val2817Ile
NM_025074.6:c.8449G>A NP_079350.5:p.Val2817Ile
XM_006714314.1:c.8443G>A XP_006714377.1:p.Val2815Ile
XM_006714316.1:c.8221G>A XP_006714379.1:p.Val2741Ile
XM_011532270.1:c.6148G>A XP_011530572.1:p.Val2050Ile
XM_011532271.1:c.3337G>A XP_011530573.1:p.Val1113Ile
XM_006714316.3:c.8221G>A XP_006714379.1:p.Val2741Ile
NM_025074.7:c.8449G>A MANE Select NP_079350.5:p.Val2817Ile