Canonical Allele Identifier: CA357388638

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78441163T>C , CM000666.2:g.78441163T>C	GRCh38
NC_000004.11:g.79362317T>C , CM000666.1:g.79362317T>C	GRCh37
NC_000004.10:g.79581341T>C	NCBI36
NG_015812.1:g.388594T>C
NG_015812.2:g.388594T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325942.11:c.5531T>C	ENSP00000326330.6:p.Val1844Ala
ENST00000682513.1:c.5531T>C	ENSP00000508201.1:p.Val1844Ala
ENST00000684159.1:c.5531T>C	ENSP00000506875.1:p.Val1844Ala
ENST00000512123.4:c.5531T>C MANE Select	ENSP00000422834.2:p.Val1844Ala
ENST00000264899.10:c.845-2940T>C	ENSP00000264899.7:n.845-2940T>C
ENST00000325942.10:c.5531T>C	ENSP00000326330.6:p.Val1844Ala
ENST00000510944.3:c.879T>C
ENST00000512123.3:c.5531T>C	ENSP00000422834.2:p.Val1844Ala
NM_001166133.1:c.5531T>C	NP_001159605.1:p.Val1844Ala
NM_025074.6:c.5531T>C	NP_079350.5:p.Val1844Ala
XM_006714314.1:c.5525T>C	XP_006714377.1:p.Val1842Ala
XM_006714316.1:c.5531T>C	XP_006714379.1:p.Val1844Ala
XM_011532270.1:c.3230T>C	XP_011530572.1:p.Val1077Ala
XM_011532271.1:c.419T>C	XP_011530573.1:p.Val140Ala
XM_006714316.3:c.5531T>C	XP_006714379.1:p.Val1844Ala
NM_025074.7:c.5531T>C MANE Select	NP_079350.5:p.Val1844Ala
NM_001166133.2:c.5531T>C	NP_001159605.1:p.Val1844Ala