Canonical Allele Identifier: CA352442574

Gene: FYCO1

Linked Data

• MyVariant Identifiers: chr3:g.46021222A>C (hg19) ; chr3:g.45979730A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45979730A>C , CM000665.2:g.45979730A>C	GRCh38
NC_000003.11:g.46021222A>C , CM000665.1:g.46021222A>C	GRCh37
NC_000003.10:g.45996226A>C	NCBI36
NG_031955.1:g.21095T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000296137.7:c.263T>G MANE Select	ENSP00000296137.2:p.Ile88Ser
ENST00000296137.6:c.263T>G	ENSP00000296137.2:p.Ile88Ser
ENST00000535325.5:c.263T>G	ENSP00000441178.1:p.Ile88Ser
NM_024513.3:c.263T>G	NP_078789.2:p.Ile88Ser
XM_006713333.2:c.263T>G	XP_006713396.1:p.Ile88Ser
XM_006713334.2:c.263T>G	XP_006713397.1:p.Ile88Ser
XM_011534111.1:c.263T>G	XP_011532413.1:p.Ile88Ser
XM_011534112.1:c.263T>G	XP_011532414.1:p.Ile88Ser
XR_245157.1:n.478T>G
XM_006713333.3:c.263T>G	XP_006713396.1:p.Ile88Ser
XM_006713334.3:c.263T>G	XP_006713397.1:p.Ile88Ser
XM_011534111.3:c.263T>G	XP_011532413.1:p.Ile88Ser
XR_001740265.1:n.478T>G
NM_024513.4:c.263T>G MANE Select	NP_078789.2:p.Ile88Ser
NM_001386421.1:c.263T>G	NP_001373350.1:p.Ile88Ser
NM_001386422.1:c.263T>G	NP_001373351.1:p.Ile88Ser
NM_001386423.1:c.263T>G	NP_001373352.1:p.Ile88Ser
NM_001386424.1:c.263T>G	NP_001373353.1:p.Ile88Ser
NM_001386425.1:c.263T>G	NP_001373354.1:p.Ile88Ser
NM_001386426.1:c.143T>G	NP_001373355.1:p.Ile48Ser
NM_001386427.1:c.263T>G	NP_001373356.1:p.Ile88Ser
NM_001386428.1:c.263T>G	NP_001373357.1:p.Ile88Ser
NM_001386429.1:c.263T>G	NP_001373358.1:p.Ile88Ser
NM_001386430.1:c.-62+5126T>G	NP_001373359.1:n.-62+5126T>G
NR_170107.1:n.478T>G