Canonical Allele Identifier: CA11499350
Gene: FYCO1 HGNC NCBI

Linked Data

dbSNP Id: rs1545985

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.45963986G>A , CM000665.2:g.45963986G>A GRCh38
NC_000003.11:g.46005478G>A , CM000665.1:g.46005478G>A GRCh37
NC_000003.10:g.45980482G>A NCBI36
NG_031955.1:g.36839C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000296137.6:c.3269+350C>T ENSP00000296137.2:p.=
ENST00000535325.5:c.3269+350C>T ENSP00000441178.1:p.=
NM_024513.3:c.3269+350C>T NP_078789.2:p.=
XM_006713333.2:c.3269+350C>T XP_006713396.1:p.=
XM_006713334.2:c.3269+350C>T XP_006713397.1:p.=
XM_011534111.1:c.3269+350C>T XP_011532413.1:p.=
XM_011534112.1:c.3269+350C>T XP_011532414.1:p.=
XM_006713333.3:c.3269+350C>T XP_006713396.1:p.=
XM_006713334.3:c.3269+350C>T XP_006713397.1:p.=
XM_011534111.3:c.3269+350C>T XP_011532413.1:p.=
NM_024513.4:c.3269+350C>T MANE Select NP_078789.2:p.=
NM_001386421.1:c.3269+350C>T NP_001373350.1:p.=
NM_001386422.1:c.3269+350C>T NP_001373351.1:p.=
NM_001386423.1:c.3269+350C>T NP_001373352.1:p.=
NM_001386424.1:c.3269+350C>T NP_001373353.1:p.=
NM_001386425.1:c.3269+350C>T NP_001373354.1:p.=
NM_001386426.1:c.3149+350C>T NP_001373355.1:p.=
NM_001386427.1:c.3125+350C>T NP_001373356.1:p.=
NM_001386428.1:c.3269+350C>T NP_001373357.1:p.=
NM_001386429.1:c.3269+350C>T NP_001373358.1:p.=
NM_001386430.1:c.2669+350C>T NP_001373359.1:p.=