Canonical Allele Identifier: CA2580069868

Gene: FYCO1

Linked Data

• ClinVar Variation Id: 1709262
• ClinVar RCV Id: RCV002289077

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45979726_45979728delinsTCA , CM000665.2:g.45979726_45979728delinsTCA	GRCh38
NC_000003.11:g.46021218_46021220delinsTCA , CM000665.1:g.46021218_46021220delinsTCA	GRCh37
NC_000003.10:g.45996222_45996224delinsTCA	NCBI36
NG_031955.1:g.21097_21099delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296137.7:c.265_267delinsTGA MANE Select	ENSP00000296137.2:p.Arg89Ter
ENST00000296137.6:c.265_267delinsTGA	ENSP00000296137.2:p.Arg89Ter
ENST00000535325.5:c.265_267delinsTGA	ENSP00000441178.1:p.Arg89Ter
NM_024513.3:c.265_267delinsTGA	NP_078789.2:p.Arg89Ter
XM_006713333.2:c.265_267delinsTGA	XP_006713396.1:p.Arg89Ter
XM_006713334.2:c.265_267delinsTGA	XP_006713397.1:p.Arg89Ter
XM_011534111.1:c.265_267delinsTGA	XP_011532413.1:p.Arg89Ter
XM_011534112.1:c.265_267delinsTGA	XP_011532414.1:p.Arg89Ter
XR_245157.1:n.480_482delinsTGA
XM_006713333.3:c.265_267delinsTGA	XP_006713396.1:p.Arg89Ter
XM_006713334.3:c.265_267delinsTGA	XP_006713397.1:p.Arg89Ter
XM_011534111.3:c.265_267delinsTGA	XP_011532413.1:p.Arg89Ter
XR_001740265.1:n.480_482delinsTGA
NM_024513.4:c.265_267delinsTGA MANE Select	NP_078789.2:p.Arg89Ter
NM_001386421.1:c.265_267delinsTGA	NP_001373350.1:p.Arg89Ter
NM_001386422.1:c.265_267delinsTGA	NP_001373351.1:p.Arg89Ter
NM_001386423.1:c.265_267delinsTGA	NP_001373352.1:p.Arg89Ter
NM_001386424.1:c.265_267delinsTGA	NP_001373353.1:p.Arg89Ter
NM_001386425.1:c.265_267delinsTGA	NP_001373354.1:p.Arg89Ter
NM_001386426.1:c.145_147delinsTGA	NP_001373355.1:p.Arg49Ter
NM_001386427.1:c.265_267delinsTGA	NP_001373356.1:p.Arg89Ter
NM_001386428.1:c.265_267delinsTGA	NP_001373357.1:p.Arg89Ter
NM_001386429.1:c.265_267delinsTGA	NP_001373358.1:p.Arg89Ter
NM_001386430.1:c.-62+5128_-62+5130delinsTGA	NP_001373359.1:n.-62+5128_-62+5130delinsTGA
NR_170107.1:n.480_482delinsTGA