Canonical Allele Identifier: CA357372018

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78363958T>A , CM000666.2:g.78363958T>A	GRCh38
NC_000004.11:g.79285112T>A , CM000666.1:g.79285112T>A	GRCh37
NC_000004.10:g.79504136T>A	NCBI36
NG_015812.1:g.311389T>A
NG_015812.2:g.311389T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_025074.7:c.2626T>A MANE Select	NP_079350.5:p.Ser876Thr
ENST00000512123.4:c.2626T>A MANE Select	ENSP00000422834.2:p.Ser876Thr
NM_001166133.1:c.2626T>A	NP_001159605.1:p.Ser876Thr
NM_001166133.2:c.2626T>A	NP_001159605.1:p.Ser876Thr
NM_025074.6:c.2626T>A	NP_079350.5:p.Ser876Thr
ENST00000264899.10:c.845-80145T>A	ENSP00000264899.7:n.845-80145T>A
ENST00000325942.10:c.2626T>A	ENSP00000326330.6:p.Ser876Thr
ENST00000325942.11:c.2626T>A	ENSP00000326330.6:p.Ser876Thr
ENST00000512123.3:c.2626T>A	ENSP00000422834.2:p.Ser876Thr
ENST00000682513.1:c.2626T>A	ENSP00000508201.1:p.Ser876Thr
ENST00000684159.1:c.2626T>A	ENSP00000506875.1:p.Ser876Thr
XM_006714314.1:c.2626T>A	XP_006714377.1:p.Ser876Thr
XM_006714316.1:c.2626T>A	XP_006714379.1:p.Ser876Thr
XM_006714316.3:c.2626T>A	XP_006714379.1:p.Ser876Thr
XM_011532270.1:c.325T>A	XP_011530572.1:p.Ser109Thr