Canonical Allele Identifier: CA439974347

Gene: FRAS1

Linked Data

• MyVariant Identifiers: chr4:g.79328965C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78407811C>T , CM000666.2:g.78407811C>T	GRCh38
NC_000004.11:g.79328965C>T , CM000666.1:g.79328965C>T	GRCh37
NC_000004.10:g.79547989C>T	NCBI36
NG_015812.1:g.355242C>T
NG_015812.2:g.355242C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000325942.11:c.4278C>T	ENSP00000326330.6:p.Ala1426=
ENST00000682513.1:c.4278C>T	ENSP00000508201.1:p.Ala1426=
ENST00000684159.1:c.4278C>T	ENSP00000506875.1:p.Ala1426=
ENST00000512123.4:c.4278C>T MANE Select	ENSP00000422834.2:p.Ala1426=
ENST00000264899.10:c.845-36292C>T	ENSP00000264899.7:n.845-36292C>T
ENST00000325942.10:c.4278C>T	ENSP00000326330.6:p.Ala1426=
ENST00000512123.3:c.4278C>T	ENSP00000422834.2:p.Ala1426=
NM_001166133.1:c.4278C>T	NP_001159605.1:p.Ala1426=
NM_025074.6:c.4278C>T	NP_079350.5:p.Ala1426=
XM_006714314.1:c.4278C>T	XP_006714377.1:p.Ala1426=
XM_006714316.1:c.4278C>T	XP_006714379.1:p.Ala1426=
XM_011532270.1:c.1977C>T	XP_011530572.1:p.Ala659=
XM_006714316.3:c.4278C>T	XP_006714379.1:p.Ala1426=
NM_025074.7:c.4278C>T MANE Select	NP_079350.5:p.Ala1426=
NM_001166133.2:c.4278C>T	NP_001159605.1:p.Ala1426=