Canonical Allele Identifier: CA357389015

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78441243A>G , CM000666.2:g.78441243A>G	GRCh38
NC_000004.11:g.79362397A>G , CM000666.1:g.79362397A>G	GRCh37
NC_000004.10:g.79581421A>G	NCBI36
NG_015812.1:g.388674A>G
NG_015812.2:g.388674A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025074.7:c.5611A>G MANE Select	NP_079350.5:p.Ile1871Val
ENST00000512123.4:c.5611A>G MANE Select	ENSP00000422834.2:p.Ile1871Val
NM_001166133.1:c.5611A>G	NP_001159605.1:p.Ile1871Val
NM_001166133.2:c.5611A>G	NP_001159605.1:p.Ile1871Val
NM_025074.6:c.5611A>G	NP_079350.5:p.Ile1871Val
ENST00000264899.10:c.845-2860A>G	ENSP00000264899.7:n.845-2860A>G
ENST00000325942.10:c.5611A>G	ENSP00000326330.6:p.Ile1871Val
ENST00000325942.11:c.5611A>G	ENSP00000326330.6:p.Ile1871Val
ENST00000510944.3:c.959A>G
ENST00000512123.3:c.5611A>G	ENSP00000422834.2:p.Ile1871Val
ENST00000682513.1:c.5611A>G	ENSP00000508201.1:p.Ile1871Val
ENST00000684159.1:c.5611A>G	ENSP00000506875.1:p.Ile1871Val
XM_006714314.1:c.5605A>G	XP_006714377.1:p.Ile1869Val
XM_006714316.1:c.5611A>G	XP_006714379.1:p.Ile1871Val
XM_006714316.3:c.5611A>G	XP_006714379.1:p.Ile1871Val
XM_011532270.1:c.3310A>G	XP_011530572.1:p.Ile1104Val
XM_011532271.1:c.499A>G	XP_011530573.1:p.Ile167Val