Canonical Allele Identifier: CA2977589

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78445528G>A , CM000666.2:g.78445528G>A	GRCh38
NC_000004.11:g.79366682G>A , CM000666.1:g.79366682G>A	GRCh37
NC_000004.10:g.79585706G>A	NCBI36
NG_015812.1:g.392959G>A
NG_015812.2:g.392959G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325942.11:c.5672G>A	ENSP00000326330.6:p.Arg1891His
ENST00000682513.1:c.5672G>A	ENSP00000508201.1:p.Arg1891His
ENST00000684159.1:c.5672G>A	ENSP00000506875.1:p.Arg1891His
ENST00000512123.4:c.5672G>A MANE Select	ENSP00000422834.2:p.Arg1891His
ENST00000264899.10:c.*1316G>A	ENSP00000264899.7:n.*1316G>A
ENST00000325942.10:c.5672G>A	ENSP00000326330.6:p.Arg1891His
ENST00000510944.3:c.1020G>A
ENST00000512123.3:c.5672G>A	ENSP00000422834.2:p.Arg1891His
NM_001166133.1:c.5672G>A	NP_001159605.1:p.Arg1891His
NM_025074.6:c.5672G>A	NP_079350.5:p.Arg1891His
XM_006714314.1:c.5666G>A	XP_006714377.1:p.Arg1889His
XM_006714316.1:c.5672G>A	XP_006714379.1:p.Arg1891His
XM_011532270.1:c.3371G>A	XP_011530572.1:p.Arg1124His
XM_011532271.1:c.560G>A	XP_011530573.1:p.Arg187His
XM_006714316.3:c.5672G>A	XP_006714379.1:p.Arg1891His
NM_025074.7:c.5672G>A MANE Select	NP_079350.5:p.Arg1891His
NM_001166133.2:c.5672G>A	NP_001159605.1:p.Arg1891His