Canonical Allele Identifier: CA431810070

Gene: GIGYF2

Linked Data

• MyVariant Identifiers: chr2:g.233674513T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232809803T>C , CM000664.2:g.232809803T>C	GRCh38
NC_000002.11:g.233674513T>C , CM000664.1:g.233674513T>C	GRCh37
NC_000002.10:g.233382757T>C	NCBI36
NG_011847.1:g.117499T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373563.9:c.1890T>C MANE Select	ENSP00000362664.5:p.Phe630=
ENST00000676848.1:c.1236T>C	ENSP00000503313.1:p.Phe412=
ENST00000677450.1:c.1371T>C	ENSP00000503420.1:p.Phe457=
ENST00000677591.1:c.1146T>C	ENSP00000503061.1:p.Phe382=
ENST00000678230.1:c.1383T>C	ENSP00000504272.1:p.Phe461=
ENST00000678339.1:c.1146T>C	ENSP00000503437.1:p.Phe382=
ENST00000678466.1:c.1146T>C	ENSP00000504219.1:p.Phe382=
ENST00000678885.1:c.1146T>C	ENSP00000503563.1:p.Phe382=
ENST00000373563.8:c.1890T>C	ENSP00000362664.4:p.Phe630=
ENST00000409196.7:c.1872T>C	ENSP00000387070.3:p.Phe624=
ENST00000409451.7:c.1953T>C	ENSP00000387170.3:p.Phe651=
ENST00000409480.5:c.1956T>C	ENSP00000386765.1:p.Phe652=
ENST00000409547.5:c.1890T>C	ENSP00000386537.1:p.Phe630=
ENST00000423659.5:c.1719T>C	ENSP00000404195.1:p.Phe573=
ENST00000440945.5:c.1872T>C	ENSP00000410297.1:p.Phe624=
ENST00000482952.5:n.128T>C
ENST00000629305.2:c.1956T>C	ENSP00000487548.1:p.Phe652=
NM_001103146.1:c.1890T>C	NP_001096616.1:p.Phe630=
NM_001103147.1:c.1953T>C	NP_001096617.1:p.Phe651=
NM_001103148.1:c.1872T>C	NP_001096618.1:p.Phe624=
NM_015575.3:c.1890T>C	NP_056390.2:p.Phe630=
NR_103492.1:n.2003T>C
NM_001103146.3:c.1890T>C MANE Select	NP_001096616.1:p.Phe630=
NM_001103147.2:c.1953T>C	NP_001096617.1:p.Phe651=
NM_001103148.2:c.1872T>C	NP_001096618.1:p.Phe624=
NM_015575.4:c.1890T>C	NP_056390.2:p.Phe630=