Canonical Allele Identifier: CA431808084

Gene: GIGYF2

Linked Data

• MyVariant Identifiers: chr2:g.233655592A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232790882A>T , CM000664.2:g.232790882A>T	GRCh38
NC_000002.11:g.233655592A>T , CM000664.1:g.233655592A>T	GRCh37
NC_000002.10:g.233363836A>T	NCBI36
NG_011847.1:g.98578A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373563.9:c.897A>T MANE Select	ENSP00000362664.5:p.Thr299=
ENST00000676848.1:c.243A>T	ENSP00000503313.1:p.Thr81=
ENST00000677450.1:c.378A>T	ENSP00000503420.1:p.Thr126=
ENST00000677591.1:c.153A>T	ENSP00000503061.1:p.Thr51=
ENST00000678230.1:c.390A>T	ENSP00000504272.1:p.Thr130=
ENST00000678339.1:c.153A>T	ENSP00000503437.1:p.Thr51=
ENST00000678466.1:c.153A>T	ENSP00000504219.1:p.Thr51=
ENST00000678885.1:c.153A>T	ENSP00000503563.1:p.Thr51=
ENST00000373563.8:c.897A>T	ENSP00000362664.4:p.Thr299=
ENST00000409196.7:c.879A>T	ENSP00000387070.3:p.Thr293=
ENST00000409451.7:c.963A>T	ENSP00000387170.3:p.Thr321=
ENST00000409480.5:c.963A>T	ENSP00000386765.1:p.Thr321=
ENST00000409547.5:c.897A>T	ENSP00000386537.1:p.Thr299=
ENST00000410033.1:c.243A>T	ENSP00000387276.1:p.Thr81=
ENST00000423659.5:c.726A>T	ENSP00000404195.1:p.Thr242=
ENST00000424414.6:c.153A>T	ENSP00000401261.2:p.Thr51=
ENST00000427649.5:c.153A>T	ENSP00000398055.1:p.Thr51=
ENST00000436349.5:c.153A>T	ENSP00000400076.1:p.Thr51=
ENST00000440945.5:c.879A>T	ENSP00000410297.1:p.Thr293=
ENST00000455139.5:c.153A>T	ENSP00000395299.1:p.Thr51=
ENST00000458528.1:c.108-130A>T	ENSP00000389322.1:n.108-130A>T
ENST00000629305.2:c.963A>T	ENSP00000487548.1:p.Thr321=
NM_001103146.1:c.897A>T	NP_001096616.1:p.Thr299=
NM_001103147.1:c.963A>T	NP_001096617.1:p.Thr321=
NM_001103148.1:c.879A>T	NP_001096618.1:p.Thr293=
NM_015575.3:c.897A>T	NP_056390.2:p.Thr299=
NR_103492.1:n.1010A>T
NM_001103146.3:c.897A>T MANE Select	NP_001096616.1:p.Thr299=
NM_001103147.2:c.963A>T	NP_001096617.1:p.Thr321=
NM_001103148.2:c.879A>T	NP_001096618.1:p.Thr293=
NM_015575.4:c.897A>T	NP_056390.2:p.Thr299=