Canonical Allele Identifier: CA1335441885
Gene: GIGYF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232809744A= , CM000664.2:g.232809744A= GRCh38
NC_000002.11:g.233674454A= , CM000664.1:g.233674454A= GRCh37
NC_000002.10:g.233382698A= NCBI36
NG_011847.1:g.117440A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373563.9:c.1831A= MANE Select ENSP00000362664.5:p.Thr611=
ENST00000676848.1:c.1177A= ENSP00000503313.1:p.Thr393=
ENST00000677450.1:c.1312A= ENSP00000503420.1:p.Thr438=
ENST00000677591.1:c.1087A= ENSP00000503061.1:p.Thr363=
ENST00000678230.1:c.1324A= ENSP00000504272.1:p.Thr442=
ENST00000678339.1:c.1087A= ENSP00000503437.1:p.Thr363=
ENST00000678466.1:c.1087A= ENSP00000504219.1:p.Thr363=
ENST00000678885.1:c.1087A= ENSP00000503563.1:p.Thr363=
ENST00000373563.8:c.1831A= ENSP00000362664.4:p.Thr611=
ENST00000409196.7:c.1813A= ENSP00000387070.3:p.Thr605=
ENST00000409451.7:c.1894A= ENSP00000387170.3:p.Thr632=
ENST00000409480.5:c.1897A= ENSP00000386765.1:p.Thr633=
ENST00000409547.5:c.1831A= ENSP00000386537.1:p.Thr611=
ENST00000423659.5:c.1660A= ENSP00000404195.1:p.Thr554=
ENST00000440945.5:c.1813A= ENSP00000410297.1:p.Thr605=
ENST00000482952.5:n.69A=
ENST00000629305.2:c.1897A= ENSP00000487548.1:p.Thr633=
NM_001103146.1:c.1831A= NP_001096616.1:p.Thr611=
NM_001103147.1:c.1894A= NP_001096617.1:p.Thr632=
NM_001103148.1:c.1813A= NP_001096618.1:p.Thr605=
NM_015575.3:c.1831A= NP_056390.2:p.Thr611=
NR_103492.1:n.1944A=
NM_001103146.3:c.1831A= MANE Select NP_001096616.1:p.Thr611=
NM_001103147.2:c.1894A= NP_001096617.1:p.Thr632=
NM_001103148.2:c.1813A= NP_001096618.1:p.Thr605=
NM_015575.4:c.1831A= NP_056390.2:p.Thr611=