Canonical Allele Identifier: CA351011380
Gene: GIGYF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232790871G>C , CM000664.2:g.232790871G>C GRCh38
NC_000002.11:g.233655581G>C , CM000664.1:g.233655581G>C GRCh37
NC_000002.10:g.233363825G>C NCBI36
NG_011847.1:g.98567G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373563.9:c.886G>C MANE Select ENSP00000362664.5:p.Glu296Gln
ENST00000676848.1:c.232G>C ENSP00000503313.1:p.Glu78Gln
ENST00000677450.1:c.367G>C ENSP00000503420.1:p.Glu123Gln
ENST00000677591.1:c.142G>C ENSP00000503061.1:p.Glu48Gln
ENST00000678230.1:c.379G>C ENSP00000504272.1:p.Glu127Gln
ENST00000678339.1:c.142G>C ENSP00000503437.1:p.Glu48Gln
ENST00000678466.1:c.142G>C ENSP00000504219.1:p.Glu48Gln
ENST00000678885.1:c.142G>C ENSP00000503563.1:p.Glu48Gln
ENST00000373563.8:c.886G>C ENSP00000362664.4:p.Glu296Gln
ENST00000409196.7:c.868G>C ENSP00000387070.3:p.Glu290Gln
ENST00000409451.7:c.952G>C ENSP00000387170.3:p.Glu318Gln
ENST00000409480.5:c.952G>C ENSP00000386765.1:p.Glu318Gln
ENST00000409547.5:c.886G>C ENSP00000386537.1:p.Glu296Gln
ENST00000410033.1:c.232G>C ENSP00000387276.1:p.Glu78Gln
ENST00000423659.5:c.715G>C ENSP00000404195.1:p.Glu239Gln
ENST00000424414.6:c.142G>C ENSP00000401261.2:p.Glu48Gln
ENST00000427649.5:c.142G>C ENSP00000398055.1:p.Glu48Gln
ENST00000436349.5:c.142G>C ENSP00000400076.1:p.Glu48Gln
ENST00000440945.5:c.868G>C ENSP00000410297.1:p.Glu290Gln
ENST00000455139.5:c.142G>C ENSP00000395299.1:p.Glu48Gln
ENST00000458528.1:c.107+125G>C ENSP00000389322.1:n.107+125G>C
ENST00000629305.2:c.952G>C ENSP00000487548.1:p.Glu318Gln
NM_001103146.1:c.886G>C NP_001096616.1:p.Glu296Gln
NM_001103147.1:c.952G>C NP_001096617.1:p.Glu318Gln
NM_001103148.1:c.868G>C NP_001096618.1:p.Glu290Gln
NM_015575.3:c.886G>C NP_056390.2:p.Glu296Gln
NR_103492.1:n.999G>C
NM_001103146.3:c.886G>C MANE Select NP_001096616.1:p.Glu296Gln
NM_001103147.2:c.952G>C NP_001096617.1:p.Glu318Gln
NM_001103148.2:c.868G>C NP_001096618.1:p.Glu290Gln
NM_015575.4:c.886G>C NP_056390.2:p.Glu296Gln