Canonical Allele Identifier: CA1361909891

Gene: FYCO1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45979726G= , CM000665.2:g.45979726G=	GRCh38
NC_000003.11:g.46021218G= , CM000665.1:g.46021218G=	GRCh37
NC_000003.10:g.45996222G=	NCBI36
NG_031955.1:g.21099C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296137.7:c.267C= MANE Select	ENSP00000296137.2:p.Arg89=
ENST00000296137.6:c.267C=	ENSP00000296137.2:p.Arg89=
ENST00000535325.5:c.267C=	ENSP00000441178.1:p.Arg89=
NM_024513.3:c.267C=	NP_078789.2:p.Arg89=
XM_006713333.2:c.267C=	XP_006713396.1:p.Arg89=
XM_006713334.2:c.267C=	XP_006713397.1:p.Arg89=
XM_011534111.1:c.267C=	XP_011532413.1:p.Arg89=
XM_011534112.1:c.267C=	XP_011532414.1:p.Arg89=
XR_245157.1:n.482C=
XM_006713333.3:c.267C=	XP_006713396.1:p.Arg89=
XM_006713334.3:c.267C=	XP_006713397.1:p.Arg89=
XM_011534111.3:c.267C=	XP_011532413.1:p.Arg89=
XR_001740265.1:n.482C=
NM_024513.4:c.267C= MANE Select	NP_078789.2:p.Arg89=
NM_001386421.1:c.267C=	NP_001373350.1:p.Arg89=
NM_001386422.1:c.267C=	NP_001373351.1:p.Arg89=
NM_001386423.1:c.267C=	NP_001373352.1:p.Arg89=
NM_001386424.1:c.267C=	NP_001373353.1:p.Arg89=
NM_001386425.1:c.267C=	NP_001373354.1:p.Arg89=
NM_001386426.1:c.147C=	NP_001373355.1:p.Arg49=
NM_001386427.1:c.267C=	NP_001373356.1:p.Arg89=
NM_001386428.1:c.267C=	NP_001373357.1:p.Arg89=
NM_001386429.1:c.267C=	NP_001373358.1:p.Arg89=
NM_001386430.1:c.-62+5130C=	NP_001373359.1:n.-62+5130C=
NR_170107.1:n.482C=