Canonical Allele Identifier: CA1470510438

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78407815G= , CM000666.2:g.78407815G=	GRCh38
NC_000004.11:g.79328969G= , CM000666.1:g.79328969G=	GRCh37
NC_000004.10:g.79547993G=	NCBI36
NG_015812.1:g.355246G=
NG_015812.2:g.355246G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000325942.11:c.4282G=	ENSP00000326330.6:p.Ala1428=
ENST00000682513.1:c.4282G=	ENSP00000508201.1:p.Ala1428=
ENST00000684159.1:c.4282G=	ENSP00000506875.1:p.Ala1428=
ENST00000512123.4:c.4282G= MANE Select	ENSP00000422834.2:p.Ala1428=
ENST00000264899.10:c.845-36288G=	ENSP00000264899.7:n.845-36288G=
ENST00000325942.10:c.4282G=	ENSP00000326330.6:p.Ala1428=
ENST00000512123.3:c.4282G=	ENSP00000422834.2:p.Ala1428=
NM_001166133.1:c.4282G=	NP_001159605.1:p.Ala1428=
NM_025074.6:c.4282G=	NP_079350.5:p.Ala1428=
XM_006714314.1:c.4282G=	XP_006714377.1:p.Ala1428=
XM_006714316.1:c.4282G=	XP_006714379.1:p.Ala1428=
XM_011532270.1:c.1981G=	XP_011530572.1:p.Ala661=
XM_006714316.3:c.4282G=	XP_006714379.1:p.Ala1428=
NM_025074.7:c.4282G= MANE Select	NP_079350.5:p.Ala1428=
NM_001166133.2:c.4282G=	NP_001159605.1:p.Ala1428=