Canonical Allele Identifier: CA2978866
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78513507G>A , CM000666.2:g.78513507G>A GRCh38
NC_000004.11:g.79434661G>A , CM000666.1:g.79434661G>A GRCh37
NC_000004.10:g.79653685G>A NCBI36
NG_015812.1:g.460938G>A
NG_015812.2:g.460938G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000512123.4:c.10129G>A MANE Select ENSP00000422834.2:p.Val3377Ile
ENST00000512123.3:c.10129G>A ENSP00000422834.2:p.Val3377Ile
NM_025074.6:c.10129G>A NP_079350.5:p.Val3377Ile
XM_006714314.1:c.10123G>A XP_006714377.1:p.Val3375Ile
XM_006714316.1:c.9901G>A XP_006714379.1:p.Val3301Ile
XM_011532270.1:c.7828G>A XP_011530572.1:p.Val2610Ile
XM_011532271.1:c.5017G>A XP_011530573.1:p.Val1673Ile
XM_006714316.3:c.9901G>A XP_006714379.1:p.Val3301Ile
NM_025074.7:c.10129G>A MANE Select NP_079350.5:p.Val3377Ile