Canonical Allele Identifier: CA2353537
Gene: FYCO1 HGNC NCBI

Linked Data

dbSNP Id: rs376736854
gnomAD v2: 3-46021197-C-G
gnomAD v4: 3-45979705-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.45979705C>G , CM000665.2:g.45979705C>G GRCh38
NC_000003.11:g.46021197C>G , CM000665.1:g.46021197C>G GRCh37
NC_000003.10:g.45996201C>G NCBI36
NG_031955.1:g.21120G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296137.7:c.288G>C MANE Select ENSP00000296137.2:p.Glu96Asp
ENST00000296137.6:c.288G>C ENSP00000296137.2:p.Glu96Asp
ENST00000535325.5:c.288G>C ENSP00000441178.1:p.Glu96Asp
NM_024513.3:c.288G>C NP_078789.2:p.Glu96Asp
XM_006713333.2:c.288G>C XP_006713396.1:p.Glu96Asp
XM_006713334.2:c.288G>C XP_006713397.1:p.Glu96Asp
XM_011534111.1:c.288G>C XP_011532413.1:p.Glu96Asp
XM_011534112.1:c.288G>C XP_011532414.1:p.Glu96Asp
XR_245157.1:n.503G>C
XM_006713333.3:c.288G>C XP_006713396.1:p.Glu96Asp
XM_006713334.3:c.288G>C XP_006713397.1:p.Glu96Asp
XM_011534111.3:c.288G>C XP_011532413.1:p.Glu96Asp
XR_001740265.1:n.503G>C
NM_024513.4:c.288G>C MANE Select NP_078789.2:p.Glu96Asp
NM_001386421.1:c.288G>C NP_001373350.1:p.Glu96Asp
NM_001386422.1:c.288G>C NP_001373351.1:p.Glu96Asp
NM_001386423.1:c.288G>C NP_001373352.1:p.Glu96Asp
NM_001386424.1:c.288G>C NP_001373353.1:p.Glu96Asp
NM_001386425.1:c.288G>C NP_001373354.1:p.Glu96Asp
NM_001386426.1:c.168G>C NP_001373355.1:p.Glu56Asp
NM_001386427.1:c.288G>C NP_001373356.1:p.Glu96Asp
NM_001386428.1:c.288G>C NP_001373357.1:p.Glu96Asp
NM_001386429.1:c.288G>C NP_001373358.1:p.Glu96Asp
NM_001386430.1:c.-62+5151G>C NP_001373359.1:n.-62+5151G>C
NR_170107.1:n.503G>C