Canonical Allele Identifier: CA1335433578
Gene: GIGYF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232791434A= , CM000664.2:g.232791434A= GRCh38
NC_000002.11:g.233656144A= , CM000664.1:g.233656144A= GRCh37
NC_000002.10:g.233364388A= NCBI36
NG_011847.1:g.99130A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373563.9:c.1270A= MANE Select ENSP00000362664.5:p.Ser424=
ENST00000676848.1:c.616A= ENSP00000503313.1:p.Ser206=
ENST00000677450.1:c.751A= ENSP00000503420.1:p.Ser251=
ENST00000677591.1:c.526A= ENSP00000503061.1:p.Ser176=
ENST00000678230.1:c.763A= ENSP00000504272.1:p.Ser255=
ENST00000678339.1:c.526A= ENSP00000503437.1:p.Ser176=
ENST00000678466.1:c.526A= ENSP00000504219.1:p.Ser176=
ENST00000678885.1:c.526A= ENSP00000503563.1:p.Ser176=
ENST00000373563.8:c.1270A= ENSP00000362664.4:p.Ser424=
ENST00000409196.7:c.1252A= ENSP00000387070.3:p.Ser418=
ENST00000409451.7:c.1333A= ENSP00000387170.3:p.Ser445=
ENST00000409480.5:c.1336A= ENSP00000386765.1:p.Ser446=
ENST00000409547.5:c.1270A= ENSP00000386537.1:p.Ser424=
ENST00000423659.5:c.1099A= ENSP00000404195.1:p.Ser367=
ENST00000440945.5:c.1252A= ENSP00000410297.1:p.Ser418=
ENST00000458528.1:c.*263A= ENSP00000389322.1:n.*263A=
ENST00000629305.2:c.1336A= ENSP00000487548.1:p.Ser446=
NM_001103146.1:c.1270A= NP_001096616.1:p.Ser424=
NM_001103147.1:c.1333A= NP_001096617.1:p.Ser445=
NM_001103148.1:c.1252A= NP_001096618.1:p.Ser418=
NM_015575.3:c.1270A= NP_056390.2:p.Ser424=
NR_103492.1:n.1383A=
NM_001103146.3:c.1270A= MANE Select NP_001096616.1:p.Ser424=
NM_001103147.2:c.1333A= NP_001096617.1:p.Ser445=
NM_001103148.2:c.1252A= NP_001096618.1:p.Ser418=
NM_015575.4:c.1270A= NP_056390.2:p.Ser424=