Canonical Allele Identifier: CA357377930

Gene: FRAS1

Linked Data

• MyVariant Identifiers: chr4:g.79328854C>A (hg19) ; chr4:g.78407700C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78407700C>A , CM000666.2:g.78407700C>A	GRCh38
NC_000004.11:g.79328854C>A , CM000666.1:g.79328854C>A	GRCh37
NC_000004.10:g.79547878C>A	NCBI36
NG_015812.1:g.355131C>A
NG_015812.2:g.355131C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325942.11:c.4167C>A	ENSP00000326330.6:p.Ser1389Arg
ENST00000682513.1:c.4167C>A	ENSP00000508201.1:p.Ser1389Arg
ENST00000684159.1:c.4167C>A	ENSP00000506875.1:p.Ser1389Arg
ENST00000512123.4:c.4167C>A MANE Select	ENSP00000422834.2:p.Ser1389Arg
ENST00000264899.10:c.845-36403C>A	ENSP00000264899.7:n.845-36403C>A
ENST00000325942.10:c.4167C>A	ENSP00000326330.6:p.Ser1389Arg
ENST00000512123.3:c.4167C>A	ENSP00000422834.2:p.Ser1389Arg
NM_001166133.1:c.4167C>A	NP_001159605.1:p.Ser1389Arg
NM_025074.6:c.4167C>A	NP_079350.5:p.Ser1389Arg
XM_006714314.1:c.4167C>A	XP_006714377.1:p.Ser1389Arg
XM_006714316.1:c.4167C>A	XP_006714379.1:p.Ser1389Arg
XM_011532270.1:c.1866C>A	XP_011530572.1:p.Ser622Arg
XM_006714316.3:c.4167C>A	XP_006714379.1:p.Ser1389Arg
NM_025074.7:c.4167C>A MANE Select	NP_079350.5:p.Ser1389Arg
NM_001166133.2:c.4167C>A	NP_001159605.1:p.Ser1389Arg