Canonical Allele Identifier: CA1335433331
Gene: GIGYF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232790864T= , CM000664.2:g.232790864T= GRCh38
NC_000002.11:g.233655574T= , CM000664.1:g.233655574T= GRCh37
NC_000002.10:g.233363818T= NCBI36
NG_011847.1:g.98560T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373563.9:c.879T= MANE Select ENSP00000362664.5:p.Ala293=
ENST00000676848.1:c.225T= ENSP00000503313.1:p.Ala75=
ENST00000677450.1:c.360T= ENSP00000503420.1:p.Ala120=
ENST00000677591.1:c.135T= ENSP00000503061.1:p.Ala45=
ENST00000678230.1:c.372T= ENSP00000504272.1:p.Ala124=
ENST00000678339.1:c.135T= ENSP00000503437.1:p.Ala45=
ENST00000678466.1:c.135T= ENSP00000504219.1:p.Ala45=
ENST00000678885.1:c.135T= ENSP00000503563.1:p.Ala45=
ENST00000373563.8:c.879T= ENSP00000362664.4:p.Ala293=
ENST00000409196.7:c.861T= ENSP00000387070.3:p.Ala287=
ENST00000409451.7:c.945T= ENSP00000387170.3:p.Ala315=
ENST00000409480.5:c.945T= ENSP00000386765.1:p.Ala315=
ENST00000409547.5:c.879T= ENSP00000386537.1:p.Ala293=
ENST00000410033.1:c.225T= ENSP00000387276.1:p.Ala75=
ENST00000423659.5:c.708T= ENSP00000404195.1:p.Ala236=
ENST00000424414.6:c.135T= ENSP00000401261.2:p.Ala45=
ENST00000427649.5:c.135T= ENSP00000398055.1:p.Ala45=
ENST00000436349.5:c.135T= ENSP00000400076.1:p.Ala45=
ENST00000440945.5:c.861T= ENSP00000410297.1:p.Ala287=
ENST00000455139.5:c.135T= ENSP00000395299.1:p.Ala45=
ENST00000458528.1:c.107+118T= ENSP00000389322.1:n.107+118T=
ENST00000629305.2:c.945T= ENSP00000487548.1:p.Ala315=
NM_001103146.1:c.879T= NP_001096616.1:p.Ala293=
NM_001103147.1:c.945T= NP_001096617.1:p.Ala315=
NM_001103148.1:c.861T= NP_001096618.1:p.Ala287=
NM_015575.3:c.879T= NP_056390.2:p.Ala293=
NR_103492.1:n.992T=
NM_001103146.3:c.879T= MANE Select NP_001096616.1:p.Ala293=
NM_001103147.2:c.945T= NP_001096617.1:p.Ala315=
NM_001103148.2:c.861T= NP_001096618.1:p.Ala287=
NM_015575.4:c.879T= NP_056390.2:p.Ala293=