Canonical Allele Identifier: CA1335441886
Gene: GIGYF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232809754A= , CM000664.2:g.232809754A= GRCh38
NC_000002.11:g.233674464A= , CM000664.1:g.233674464A= GRCh37
NC_000002.10:g.233382708A= NCBI36
NG_011847.1:g.117450A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373563.9:c.1841A= MANE Select ENSP00000362664.5:p.Gln614=
ENST00000676848.1:c.1187A= ENSP00000503313.1:p.Gln396=
ENST00000677450.1:c.1322A= ENSP00000503420.1:p.Gln441=
ENST00000677591.1:c.1097A= ENSP00000503061.1:p.Gln366=
ENST00000678230.1:c.1334A= ENSP00000504272.1:p.Gln445=
ENST00000678339.1:c.1097A= ENSP00000503437.1:p.Gln366=
ENST00000678466.1:c.1097A= ENSP00000504219.1:p.Gln366=
ENST00000678885.1:c.1097A= ENSP00000503563.1:p.Gln366=
ENST00000373563.8:c.1841A= ENSP00000362664.4:p.Gln614=
ENST00000409196.7:c.1823A= ENSP00000387070.3:p.Gln608=
ENST00000409451.7:c.1904A= ENSP00000387170.3:p.Gln635=
ENST00000409480.5:c.1907A= ENSP00000386765.1:p.Gln636=
ENST00000409547.5:c.1841A= ENSP00000386537.1:p.Gln614=
ENST00000423659.5:c.1670A= ENSP00000404195.1:p.Gln557=
ENST00000440945.5:c.1823A= ENSP00000410297.1:p.Gln608=
ENST00000482952.5:n.79A=
ENST00000629305.2:c.1907A= ENSP00000487548.1:p.Gln636=
NM_001103146.1:c.1841A= NP_001096616.1:p.Gln614=
NM_001103147.1:c.1904A= NP_001096617.1:p.Gln635=
NM_001103148.1:c.1823A= NP_001096618.1:p.Gln608=
NM_015575.3:c.1841A= NP_056390.2:p.Gln614=
NR_103492.1:n.1954A=
NM_001103146.3:c.1841A= MANE Select NP_001096616.1:p.Gln614=
NM_001103147.2:c.1904A= NP_001096617.1:p.Gln635=
NM_001103148.2:c.1823A= NP_001096618.1:p.Gln608=
NM_015575.4:c.1841A= NP_056390.2:p.Gln614=