Canonical Allele Identifier: CA2979014
Gene: FRAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78521577T>C , CM000666.2:g.78521577T>C GRCh38
NC_000004.11:g.79442731T>C , CM000666.1:g.79442731T>C GRCh37
NC_000004.10:g.79661755T>C NCBI36
NG_015812.1:g.469008T>C
NG_015812.2:g.469008T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000512123.4:c.10595T>C MANE Select ENSP00000422834.2:p.Ile3532Thr
ENST00000512123.3:c.10595T>C ENSP00000422834.2:p.Ile3532Thr
NM_025074.6:c.10595T>C NP_079350.5:p.Ile3532Thr
XM_006714314.1:c.10589T>C XP_006714377.1:p.Ile3530Thr
XM_006714316.1:c.10367T>C XP_006714379.1:p.Ile3456Thr
XM_011532270.1:c.8294T>C XP_011530572.1:p.Ile2765Thr
XM_011532271.1:c.5483T>C XP_011530573.1:p.Ile1828Thr
XM_006714316.3:c.10367T>C XP_006714379.1:p.Ile3456Thr
NM_025074.7:c.10595T>C MANE Select NP_079350.5:p.Ile3532Thr