Canonical Allele Identifier: CA351019076
Gene: GIGYF2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000373563.9:c.1887G>T MANE Select ENSP00000362664.5:p.Gln629His
ENST00000676848.1:c.1233G>T ENSP00000503313.1:p.Gln411His
ENST00000677450.1:c.1368G>T ENSP00000503420.1:p.Gln456His
ENST00000677591.1:c.1143G>T ENSP00000503061.1:p.Gln381His
ENST00000678230.1:c.1380G>T ENSP00000504272.1:p.Gln460His
ENST00000678339.1:c.1143G>T ENSP00000503437.1:p.Gln381His
ENST00000678466.1:c.1143G>T ENSP00000504219.1:p.Gln381His
ENST00000678885.1:c.1143G>T ENSP00000503563.1:p.Gln381His
ENST00000373563.8:c.1887G>T ENSP00000362664.4:p.Gln629His
ENST00000409196.7:c.1869G>T ENSP00000387070.3:p.Gln623His
ENST00000409451.7:c.1950G>T ENSP00000387170.3:p.Gln650His
ENST00000409480.5:c.1953G>T ENSP00000386765.1:p.Gln651His
ENST00000409547.5:c.1887G>T ENSP00000386537.1:p.Gln629His
ENST00000423659.5:c.1716G>T ENSP00000404195.1:p.Gln572His
ENST00000440945.5:c.1869G>T ENSP00000410297.1:p.Gln623His
ENST00000482952.5:n.125G>T
ENST00000629305.2:c.1953G>T ENSP00000487548.1:p.Gln651His
NM_001103146.1:c.1887G>T NP_001096616.1:p.Gln629His
NM_001103147.1:c.1950G>T NP_001096617.1:p.Gln650His
NM_001103148.1:c.1869G>T NP_001096618.1:p.Gln623His
NM_015575.3:c.1887G>T NP_056390.2:p.Gln629His
NR_103492.1:n.2000G>T
NM_001103146.3:c.1887G>T MANE Select NP_001096616.1:p.Gln629His
NM_001103147.2:c.1950G>T NP_001096617.1:p.Gln650His
NM_001103148.2:c.1869G>T NP_001096618.1:p.Gln623His
NM_015575.4:c.1887G>T NP_056390.2:p.Gln629His