Canonical Allele Identifier: CA440225202

Gene: FRAS1

Linked Data

• MyVariant Identifiers: chr4:g.79432556C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78511402C>T , CM000666.2:g.78511402C>T	GRCh38
NC_000004.11:g.79432556C>T , CM000666.1:g.79432556C>T	GRCh37
NC_000004.10:g.79651580C>T	NCBI36
NG_015812.1:g.458833C>T
NG_015812.2:g.458833C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682513.1:c.9909C>T	ENSP00000508201.1:p.Ile3303=
ENST00000512123.4:c.9909C>T MANE Select	ENSP00000422834.2:p.Ile3303=
ENST00000512123.3:c.9909C>T	ENSP00000422834.2:p.Ile3303=
NM_025074.6:c.9909C>T	NP_079350.5:p.Ile3303=
XM_006714314.1:c.9903C>T	XP_006714377.1:p.Ile3301=
XM_006714316.1:c.9681C>T	XP_006714379.1:p.Ile3227=
XM_011532270.1:c.7608C>T	XP_011530572.1:p.Ile2536=
XM_011532271.1:c.4797C>T	XP_011530573.1:p.Ile1599=
XM_006714316.3:c.9681C>T	XP_006714379.1:p.Ile3227=
NM_025074.7:c.9909C>T MANE Select	NP_079350.5:p.Ile3303=