Canonical Allele Identifier: CA357382445

Gene: FRAS1

Linked Data

• MyVariant Identifiers: chr4:g.79432552C>A (hg19) ; chr4:g.78511398C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78511398C>A , CM000666.2:g.78511398C>A	GRCh38
NC_000004.11:g.79432552C>A , CM000666.1:g.79432552C>A	GRCh37
NC_000004.10:g.79651576C>A	NCBI36
NG_015812.1:g.458829C>A
NG_015812.2:g.458829C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682513.1:c.9905C>A	ENSP00000508201.1:p.Ala3302Asp
ENST00000512123.4:c.9905C>A MANE Select	ENSP00000422834.2:p.Ala3302Asp
ENST00000512123.3:c.9905C>A	ENSP00000422834.2:p.Ala3302Asp
NM_025074.6:c.9905C>A	NP_079350.5:p.Ala3302Asp
XM_006714314.1:c.9899C>A	XP_006714377.1:p.Ala3300Asp
XM_006714316.1:c.9677C>A	XP_006714379.1:p.Ala3226Asp
XM_011532270.1:c.7604C>A	XP_011530572.1:p.Ala2535Asp
XM_011532271.1:c.4793C>A	XP_011530573.1:p.Ala1598Asp
XM_006714316.3:c.9677C>A	XP_006714379.1:p.Ala3226Asp
NM_025074.7:c.9905C>A MANE Select	NP_079350.5:p.Ala3302Asp