Canonical Allele Identifier: CA1335441901
Gene: GIGYF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232809800G= , CM000664.2:g.232809800G= GRCh38
NC_000002.11:g.233674510G= , CM000664.1:g.233674510G= GRCh37
NC_000002.10:g.233382754G= NCBI36
NG_011847.1:g.117496G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373563.9:c.1887G= MANE Select ENSP00000362664.5:p.Gln629=
ENST00000676848.1:c.1233G= ENSP00000503313.1:p.Gln411=
ENST00000677450.1:c.1368G= ENSP00000503420.1:p.Gln456=
ENST00000677591.1:c.1143G= ENSP00000503061.1:p.Gln381=
ENST00000678230.1:c.1380G= ENSP00000504272.1:p.Gln460=
ENST00000678339.1:c.1143G= ENSP00000503437.1:p.Gln381=
ENST00000678466.1:c.1143G= ENSP00000504219.1:p.Gln381=
ENST00000678885.1:c.1143G= ENSP00000503563.1:p.Gln381=
ENST00000373563.8:c.1887G= ENSP00000362664.4:p.Gln629=
ENST00000409196.7:c.1869G= ENSP00000387070.3:p.Gln623=
ENST00000409451.7:c.1950G= ENSP00000387170.3:p.Gln650=
ENST00000409480.5:c.1953G= ENSP00000386765.1:p.Gln651=
ENST00000409547.5:c.1887G= ENSP00000386537.1:p.Gln629=
ENST00000423659.5:c.1716G= ENSP00000404195.1:p.Gln572=
ENST00000440945.5:c.1869G= ENSP00000410297.1:p.Gln623=
ENST00000482952.5:n.125G=
ENST00000629305.2:c.1953G= ENSP00000487548.1:p.Gln651=
NM_001103146.1:c.1887G= NP_001096616.1:p.Gln629=
NM_001103147.1:c.1950G= NP_001096617.1:p.Gln650=
NM_001103148.1:c.1869G= NP_001096618.1:p.Gln623=
NM_015575.3:c.1887G= NP_056390.2:p.Gln629=
NR_103492.1:n.2000G=
NM_001103146.3:c.1887G= MANE Select NP_001096616.1:p.Gln629=
NM_001103147.2:c.1950G= NP_001096617.1:p.Gln650=
NM_001103148.2:c.1869G= NP_001096618.1:p.Gln623=
NM_015575.4:c.1887G= NP_056390.2:p.Gln629=