Canonical Allele Identifier: CA440225084

Gene: FRAS1

Linked Data

• MyVariant Identifiers: chr4:g.79432505G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78511351G>C , CM000666.2:g.78511351G>C	GRCh38
NC_000004.11:g.79432505G>C , CM000666.1:g.79432505G>C	GRCh37
NC_000004.10:g.79651529G>C	NCBI36
NG_015812.1:g.458782G>C
NG_015812.2:g.458782G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682513.1:c.9858G>C	ENSP00000508201.1:p.Val3286=
ENST00000512123.4:c.9858G>C MANE Select	ENSP00000422834.2:p.Val3286=
ENST00000512123.3:c.9858G>C	ENSP00000422834.2:p.Val3286=
NM_025074.6:c.9858G>C	NP_079350.5:p.Val3286=
XM_006714314.1:c.9852G>C	XP_006714377.1:p.Val3284=
XM_006714316.1:c.9630G>C	XP_006714379.1:p.Val3210=
XM_011532270.1:c.7557G>C	XP_011530572.1:p.Val2519=
XM_011532271.1:c.4746G>C	XP_011530573.1:p.Val1582=
XM_006714316.3:c.9630G>C	XP_006714379.1:p.Val3210=
NM_025074.7:c.9858G>C MANE Select	NP_079350.5:p.Val3286=