Canonical Allele Identifier: CA2977998

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78466288C>T , CM000666.2:g.78466288C>T	GRCh38
NC_000004.11:g.79387442C>T , CM000666.1:g.79387442C>T	GRCh37
NC_000004.10:g.79606466C>T	NCBI36
NG_015812.1:g.413719C>T
NG_015812.2:g.413719C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682513.1:c.7110C>T	ENSP00000508201.1:p.His2370=
ENST00000512123.4:c.7110C>T MANE Select	ENSP00000422834.2:p.His2370=
ENST00000512123.3:c.7110C>T	ENSP00000422834.2:p.His2370=
NM_025074.6:c.7110C>T	NP_079350.5:p.His2370=
XM_006714314.1:c.7104C>T	XP_006714377.1:p.His2368=
XM_006714316.1:c.7029+1705C>T	XP_006714379.1:n.7029+1705C>T
XM_011532270.1:c.4809C>T	XP_011530572.1:p.His1603=
XM_011532271.1:c.1998C>T	XP_011530573.1:p.His666=
XM_006714316.3:c.7029+1705C>T	XP_006714379.1:n.7029+1705C>T
NM_025074.7:c.7110C>T MANE Select	NP_079350.5:p.His2370=