Canonical Allele Identifier: CA99957056

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78429190C>T , CM000666.2:g.78429190C>T	GRCh38
NC_000004.11:g.79350344C>T , CM000666.1:g.79350344C>T	GRCh37
NC_000004.10:g.79569368C>T	NCBI36
NG_015812.1:g.376621C>T
NG_015812.2:g.376621C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_025074.7:c.4807C>T MANE Select	NP_079350.5:p.Arg1603Trp
ENST00000512123.4:c.4807C>T MANE Select	ENSP00000422834.2:p.Arg1603Trp
NM_001166133.1:c.4807C>T	NP_001159605.1:p.Arg1603Trp
NM_001166133.2:c.4807C>T	NP_001159605.1:p.Arg1603Trp
NM_025074.6:c.4807C>T	NP_079350.5:p.Arg1603Trp
ENST00000264899.10:c.845-14913C>T	ENSP00000264899.7:n.845-14913C>T
ENST00000325942.10:c.4807C>T	ENSP00000326330.6:p.Arg1603Trp
ENST00000325942.11:c.4807C>T	ENSP00000326330.6:p.Arg1603Trp
ENST00000510944.3:c.155C>T
ENST00000512123.3:c.4807C>T	ENSP00000422834.2:p.Arg1603Trp
ENST00000682513.1:c.4807C>T	ENSP00000508201.1:p.Arg1603Trp
ENST00000684159.1:c.4807C>T	ENSP00000506875.1:p.Arg1603Trp
XM_006714314.1:c.4801C>T	XP_006714377.1:p.Arg1601Trp
XM_006714316.1:c.4807C>T	XP_006714379.1:p.Arg1603Trp
XM_006714316.3:c.4807C>T	XP_006714379.1:p.Arg1603Trp
XM_011532270.1:c.2506C>T	XP_011530572.1:p.Arg836Trp
XM_011532271.1:c.-58C>T	XP_011530573.1:n.-58C>T