Canonical Allele Identifier: CA351011422

Gene: GIGYF2

Linked Data

• MyVariant Identifiers: chr2:g.233655597A>T (hg19) ; chr2:g.232790887A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232790887A>T , CM000664.2:g.232790887A>T	GRCh38
NC_000002.11:g.233655597A>T , CM000664.1:g.233655597A>T	GRCh37
NC_000002.10:g.233363841A>T	NCBI36
NG_011847.1:g.98583A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373563.9:c.902A>T MANE Select	ENSP00000362664.5:p.Asp301Val
ENST00000676848.1:c.248A>T	ENSP00000503313.1:p.Asp83Val
ENST00000677450.1:c.383A>T	ENSP00000503420.1:p.Asp128Val
ENST00000677591.1:c.158A>T	ENSP00000503061.1:p.Asp53Val
ENST00000678230.1:c.395A>T	ENSP00000504272.1:p.Asp132Val
ENST00000678339.1:c.158A>T	ENSP00000503437.1:p.Asp53Val
ENST00000678466.1:c.158A>T	ENSP00000504219.1:p.Asp53Val
ENST00000678885.1:c.158A>T	ENSP00000503563.1:p.Asp53Val
ENST00000373563.8:c.902A>T	ENSP00000362664.4:p.Asp301Val
ENST00000409196.7:c.884A>T	ENSP00000387070.3:p.Asp295Val
ENST00000409451.7:c.968A>T	ENSP00000387170.3:p.Asp323Val
ENST00000409480.5:c.968A>T	ENSP00000386765.1:p.Asp323Val
ENST00000409547.5:c.902A>T	ENSP00000386537.1:p.Asp301Val
ENST00000410033.1:c.248A>T	ENSP00000387276.1:p.Asp83Val
ENST00000423659.5:c.731A>T	ENSP00000404195.1:p.Asp244Val
ENST00000424414.6:c.158A>T	ENSP00000401261.2:p.Asp53Val
ENST00000427649.5:c.158A>T	ENSP00000398055.1:p.Asp53Val
ENST00000436349.5:c.158A>T	ENSP00000400076.1:p.Asp53Val
ENST00000440945.5:c.884A>T	ENSP00000410297.1:p.Asp295Val
ENST00000455139.5:c.158A>T	ENSP00000395299.1:p.Asp53Val
ENST00000458528.1:c.108-125A>T	ENSP00000389322.1:n.108-125A>T
ENST00000629305.2:c.968A>T	ENSP00000487548.1:p.Asp323Val
NM_001103146.1:c.902A>T	NP_001096616.1:p.Asp301Val
NM_001103147.1:c.968A>T	NP_001096617.1:p.Asp323Val
NM_001103148.1:c.884A>T	NP_001096618.1:p.Asp295Val
NM_015575.3:c.902A>T	NP_056390.2:p.Asp301Val
NR_103492.1:n.1015A>T
NM_001103146.3:c.902A>T MANE Select	NP_001096616.1:p.Asp301Val
NM_001103147.2:c.968A>T	NP_001096617.1:p.Asp323Val
NM_001103148.2:c.884A>T	NP_001096618.1:p.Asp295Val
NM_015575.4:c.902A>T	NP_056390.2:p.Asp301Val