Canonical Allele Identifier: CA357375348
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78488929T>A , CM000666.2:g.78488929T>A GRCh38
NC_000004.11:g.79410083T>A , CM000666.1:g.79410083T>A GRCh37
NC_000004.10:g.79629107T>A NCBI36
NG_015812.1:g.436360T>A
NG_015812.2:g.436360T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682513.1:c.8807T>A ENSP00000508201.1:p.Val2936Asp
ENST00000512123.4:c.8807T>A MANE Select ENSP00000422834.2:p.Val2936Asp
ENST00000512123.3:c.8807T>A ENSP00000422834.2:p.Val2936Asp
NM_025074.6:c.8807T>A NP_079350.5:p.Val2936Asp
XM_006714314.1:c.8801T>A XP_006714377.1:p.Val2934Asp
XM_006714316.1:c.8579T>A XP_006714379.1:p.Val2860Asp
XM_011532270.1:c.6506T>A XP_011530572.1:p.Val2169Asp
XM_011532271.1:c.3695T>A XP_011530573.1:p.Val1232Asp
XM_006714316.3:c.8579T>A XP_006714379.1:p.Val2860Asp
NM_025074.7:c.8807T>A MANE Select NP_079350.5:p.Val2936Asp