Canonical Allele Identifier: CA99943307

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78255273G>A , CM000666.2:g.78255273G>A	GRCh38
NC_000004.11:g.79176427G>A , CM000666.1:g.79176427G>A	GRCh37
NC_000004.10:g.79395451G>A	NCBI36
NG_015812.1:g.202704G>A
NG_015812.2:g.202704G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_025074.7:c.501G>A MANE Select	NP_079350.5:p.Gln167=
ENST00000512123.4:c.501G>A MANE Select	ENSP00000422834.2:p.Gln167=
NM_001166133.1:c.501G>A	NP_001159605.1:p.Gln167=
NM_001166133.2:c.501G>A	NP_001159605.1:p.Gln167=
NM_025074.6:c.501G>A	NP_079350.5:p.Gln167=
ENST00000264899.10:c.501G>A	ENSP00000264899.7:p.Gln167=
ENST00000325942.10:c.501G>A	ENSP00000326330.6:p.Gln167=
ENST00000325942.11:c.501G>A	ENSP00000326330.6:p.Gln167=
ENST00000502446.5:c.287G>A
ENST00000502446.6:c.501G>A	ENSP00000423645.2:p.Gln167=
ENST00000508900.1:c.28G>A
ENST00000508900.2:c.501G>A	ENSP00000423809.2:p.Gln167=
ENST00000512123.3:c.501G>A	ENSP00000422834.2:p.Gln167=
ENST00000682513.1:c.501G>A	ENSP00000508201.1:p.Gln167=
ENST00000683711.1:n.821G>A
ENST00000684159.1:c.501G>A	ENSP00000506875.1:p.Gln167=
XM_006714314.1:c.501G>A	XP_006714377.1:p.Gln167=
XM_006714316.1:c.501G>A	XP_006714379.1:p.Gln167=
XM_006714316.3:c.501G>A	XP_006714379.1:p.Gln167=