Canonical Allele Identifier: CA1335433581

Gene: GIGYF2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232791438G= , CM000664.2:g.232791438G=	GRCh38
NC_000002.11:g.233656148G= , CM000664.1:g.233656148G=	GRCh37
NC_000002.10:g.233364392G=	NCBI36
NG_011847.1:g.99134G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373563.9:c.1274G= MANE Select	ENSP00000362664.5:p.Arg425=
ENST00000676848.1:c.620G=	ENSP00000503313.1:p.Arg207=
ENST00000677450.1:c.755G=	ENSP00000503420.1:p.Arg252=
ENST00000677591.1:c.530G=	ENSP00000503061.1:p.Arg177=
ENST00000678230.1:c.767G=	ENSP00000504272.1:p.Arg256=
ENST00000678339.1:c.530G=	ENSP00000503437.1:p.Arg177=
ENST00000678466.1:c.530G=	ENSP00000504219.1:p.Arg177=
ENST00000678885.1:c.530G=	ENSP00000503563.1:p.Arg177=
ENST00000373563.8:c.1274G=	ENSP00000362664.4:p.Arg425=
ENST00000409196.7:c.1256G=	ENSP00000387070.3:p.Arg419=
ENST00000409451.7:c.1337G=	ENSP00000387170.3:p.Arg446=
ENST00000409480.5:c.1340G=	ENSP00000386765.1:p.Arg447=
ENST00000409547.5:c.1274G=	ENSP00000386537.1:p.Arg425=
ENST00000423659.5:c.1103G=	ENSP00000404195.1:p.Arg368=
ENST00000440945.5:c.1256G=	ENSP00000410297.1:p.Arg419=
ENST00000458528.1:c.*267G=	ENSP00000389322.1:n.*267G=
ENST00000629305.2:c.1340G=	ENSP00000487548.1:p.Arg447=
NM_001103146.1:c.1274G=	NP_001096616.1:p.Arg425=
NM_001103147.1:c.1337G=	NP_001096617.1:p.Arg446=
NM_001103148.1:c.1256G=	NP_001096618.1:p.Arg419=
NM_015575.3:c.1274G=	NP_056390.2:p.Arg425=
NR_103492.1:n.1387G=
NM_001103146.3:c.1274G= MANE Select	NP_001096616.1:p.Arg425=
NM_001103147.2:c.1337G=	NP_001096617.1:p.Arg446=
NM_001103148.2:c.1256G=	NP_001096618.1:p.Arg419=
NM_015575.4:c.1274G=	NP_056390.2:p.Arg425=