Canonical Allele Identifier: CA214979

Gene: FYCO1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45931195A>G , CM000665.2:g.45931195A>G	GRCh38
NC_000003.11:g.45972687A>G , CM000665.1:g.45972687A>G	GRCh37
NC_000003.10:g.45947691A>G	NCBI36
NG_031955.1:g.69630T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691721.1:n.260T>C
ENST00000296137.7:c.4127T>C MANE Select	ENSP00000296137.2:p.Leu1376Pro
ENST00000296137.6:c.4127T>C	ENSP00000296137.2:p.Leu1376Pro
ENST00000433878.5:c.493T>C
ENST00000438446.1:c.140T>C	ENSP00000398517.1:p.Leu47Pro
ENST00000535325.5:c.4187T>C	ENSP00000441178.1:p.Leu1396Pro
NM_024513.3:c.4127T>C	NP_078789.2:p.Leu1376Pro
XM_006713333.2:c.4127T>C	XP_006713396.1:p.Leu1376Pro
XM_006713334.2:c.4127T>C	XP_006713397.1:p.Leu1376Pro
XM_011534111.1:c.4127T>C	XP_011532413.1:p.Leu1376Pro
XM_011534112.1:c.4127T>C	XP_011532414.1:p.Leu1376Pro
XR_245157.1:n.4342T>C
XM_006713333.3:c.4127T>C	XP_006713396.1:p.Leu1376Pro
XM_006713334.3:c.4127T>C	XP_006713397.1:p.Leu1376Pro
XM_011534111.3:c.4127T>C	XP_011532413.1:p.Leu1376Pro
XR_001740265.1:n.4223T>C
NM_024513.4:c.4127T>C MANE Select	NP_078789.2:p.Leu1376Pro
NM_001386421.1:c.4127T>C	NP_001373350.1:p.Leu1376Pro
NM_001386422.1:c.4127T>C	NP_001373351.1:p.Leu1376Pro
NM_001386423.1:c.4124T>C	NP_001373352.1:p.Leu1375Pro
NM_001386424.1:c.4127T>C	NP_001373353.1:p.Leu1376Pro
NM_001386425.1:c.4127T>C	NP_001373354.1:p.Leu1376Pro
NM_001386426.1:c.4007T>C	NP_001373355.1:p.Leu1336Pro
NM_001386427.1:c.3983T>C	NP_001373356.1:p.Leu1328Pro
NM_001386428.1:c.4127T>C	NP_001373357.1:p.Leu1376Pro
NM_001386429.1:c.4127T>C	NP_001373358.1:p.Leu1376Pro
NM_001386430.1:c.3527T>C	NP_001373359.1:p.Leu1176Pro
NR_170107.1:n.4342T>C