Canonical Allele Identifier: CA1470510464

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78407870G= , CM000666.2:g.78407870G=	GRCh38
NC_000004.11:g.79329024G= , CM000666.1:g.79329024G=	GRCh37
NC_000004.10:g.79548048G=	NCBI36
NG_015812.1:g.355301G=
NG_015812.2:g.355301G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325942.11:c.4308+29G=	ENSP00000326330.6:n.4308+29G=
ENST00000682513.1:c.4308+29G=	ENSP00000508201.1:n.4308+29G=
ENST00000684159.1:c.4308+29G=	ENSP00000506875.1:n.4308+29G=
ENST00000512123.4:c.4308+29G= MANE Select	ENSP00000422834.2:n.4308+29G=
ENST00000264899.10:c.845-36233G=	ENSP00000264899.7:n.845-36233G=
ENST00000325942.10:c.4308+29G=	ENSP00000326330.6:n.4308+29G=
ENST00000512123.3:c.4308+29G=	ENSP00000422834.2:n.4308+29G=
NM_001166133.1:c.4308+29G=	NP_001159605.1:n.4308+29G=
NM_025074.6:c.4308+29G=	NP_079350.5:n.4308+29G=
XM_006714314.1:c.4308+29G=	XP_006714377.1:n.4308+29G=
XM_006714316.1:c.4308+29G=	XP_006714379.1:n.4308+29G=
XM_011532270.1:c.2007+29G=	XP_011530572.1:n.2007+29G=
XM_006714316.3:c.4308+29G=	XP_006714379.1:n.4308+29G=
NM_025074.7:c.4308+29G= MANE Select	NP_079350.5:n.4308+29G=
NM_001166133.2:c.4308+29G=	NP_001159605.1:n.4308+29G=