Canonical Allele Identifier: CA1335441899

Gene: GIGYF2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232809790A= , CM000664.2:g.232809790A=	GRCh38
NC_000002.11:g.233674500A= , CM000664.1:g.233674500A=	GRCh37
NC_000002.10:g.233382744A=	NCBI36
NG_011847.1:g.117486A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373563.9:c.1877A= MANE Select	ENSP00000362664.5:p.Gln626=
ENST00000676848.1:c.1223A=	ENSP00000503313.1:p.Gln408=
ENST00000677450.1:c.1358A=	ENSP00000503420.1:p.Gln453=
ENST00000677591.1:c.1133A=	ENSP00000503061.1:p.Gln378=
ENST00000678230.1:c.1370A=	ENSP00000504272.1:p.Gln457=
ENST00000678339.1:c.1133A=	ENSP00000503437.1:p.Gln378=
ENST00000678466.1:c.1133A=	ENSP00000504219.1:p.Gln378=
ENST00000678885.1:c.1133A=	ENSP00000503563.1:p.Gln378=
ENST00000373563.8:c.1877A=	ENSP00000362664.4:p.Gln626=
ENST00000409196.7:c.1859A=	ENSP00000387070.3:p.Gln620=
ENST00000409451.7:c.1940A=	ENSP00000387170.3:p.Gln647=
ENST00000409480.5:c.1943A=	ENSP00000386765.1:p.Gln648=
ENST00000409547.5:c.1877A=	ENSP00000386537.1:p.Gln626=
ENST00000423659.5:c.1706A=	ENSP00000404195.1:p.Gln569=
ENST00000440945.5:c.1859A=	ENSP00000410297.1:p.Gln620=
ENST00000482952.5:n.115A=
ENST00000629305.2:c.1943A=	ENSP00000487548.1:p.Gln648=
NM_001103146.1:c.1877A=	NP_001096616.1:p.Gln626=
NM_001103147.1:c.1940A=	NP_001096617.1:p.Gln647=
NM_001103148.1:c.1859A=	NP_001096618.1:p.Gln620=
NM_015575.3:c.1877A=	NP_056390.2:p.Gln626=
NR_103492.1:n.1990A=
NM_001103146.3:c.1877A= MANE Select	NP_001096616.1:p.Gln626=
NM_001103147.2:c.1940A=	NP_001096617.1:p.Gln647=
NM_001103148.2:c.1859A=	NP_001096618.1:p.Gln620=
NM_015575.4:c.1877A=	NP_056390.2:p.Gln626=