Canonical Allele Identifier: CA351010828

Gene: GIGYF2

Linked Data

• MyVariant Identifiers: chr2:g.233655438A>G (hg19) ; chr2:g.232790728A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232790728A>G , CM000664.2:g.232790728A>G	GRCh38
NC_000002.11:g.233655438A>G , CM000664.1:g.233655438A>G	GRCh37
NC_000002.10:g.233363682A>G	NCBI36
NG_011847.1:g.98424A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000373563.9:c.743A>G MANE Select	ENSP00000362664.5:p.His248Arg
ENST00000676848.1:c.89A>G	ENSP00000503313.1:p.His30Arg
ENST00000677450.1:c.224A>G	ENSP00000503420.1:p.His75Arg
ENST00000677591.1:c.-2A>G	ENSP00000503061.1:n.-2A>G
ENST00000678230.1:c.236A>G	ENSP00000504272.1:p.His79Arg
ENST00000678339.1:c.-2A>G	ENSP00000503437.1:n.-2A>G
ENST00000678466.1:c.-2A>G	ENSP00000504219.1:n.-2A>G
ENST00000678885.1:c.-2A>G	ENSP00000503563.1:n.-2A>G
ENST00000373563.8:c.743A>G	ENSP00000362664.4:p.His248Arg
ENST00000409196.7:c.725A>G	ENSP00000387070.3:p.His242Arg
ENST00000409451.7:c.809A>G	ENSP00000387170.3:p.His270Arg
ENST00000409480.5:c.809A>G	ENSP00000386765.1:p.His270Arg
ENST00000409547.5:c.743A>G	ENSP00000386537.1:p.His248Arg
ENST00000410033.1:c.89A>G	ENSP00000387276.1:p.His30Arg
ENST00000421778.1:c.224A>G	ENSP00000390325.1:p.His75Arg
ENST00000423659.5:c.572A>G	ENSP00000404195.1:p.His191Arg
ENST00000424414.6:c.-2A>G	ENSP00000401261.2:n.-2A>G
ENST00000427649.5:c.-2A>G	ENSP00000398055.1:n.-2A>G
ENST00000436349.5:c.-2A>G	ENSP00000400076.1:n.-2A>G
ENST00000440945.5:c.725A>G	ENSP00000410297.1:p.His242Arg
ENST00000445650.5:c.236A>G	ENSP00000392218.1:p.His79Arg
ENST00000455139.5:c.-2A>G	ENSP00000395299.1:n.-2A>G
ENST00000458528.1:c.89A>G	ENSP00000389322.1:p.His30Arg
ENST00000629305.2:c.809A>G	ENSP00000487548.1:p.His270Arg
NM_001103146.1:c.743A>G	NP_001096616.1:p.His248Arg
NM_001103147.1:c.809A>G	NP_001096617.1:p.His270Arg
NM_001103148.1:c.725A>G	NP_001096618.1:p.His242Arg
NM_015575.3:c.743A>G	NP_056390.2:p.His248Arg
NR_103492.1:n.856A>G
NM_001103146.3:c.743A>G MANE Select	NP_001096616.1:p.His248Arg
NM_001103147.2:c.809A>G	NP_001096617.1:p.His270Arg
NM_001103148.2:c.725A>G	NP_001096618.1:p.His242Arg
NM_015575.4:c.743A>G	NP_056390.2:p.His248Arg