Canonical Allele Identifier: CA2169759

Gene: GIGYF2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232747646A>G , CM000664.2:g.232747646A>G	GRCh38
NC_000002.11:g.233612356A>G , CM000664.1:g.233612356A>G	GRCh37
NC_000002.10:g.233320600A>G	NCBI36
NG_011847.1:g.55342A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001103146.3:c.73A>G MANE Select	NP_001096616.1:p.Thr25Ala
ENST00000373563.9:c.73A>G MANE Select	ENSP00000362664.5:p.Thr25Ala
NM_001103146.1:c.73A>G	NP_001096616.1:p.Thr25Ala
NM_001103147.1:c.73A>G	NP_001096617.1:p.Thr25Ala
NM_001103147.2:c.73A>G	NP_001096617.1:p.Thr25Ala
NM_001103148.1:c.73A>G	NP_001096618.1:p.Thr25Ala
NM_001103148.2:c.73A>G	NP_001096618.1:p.Thr25Ala
NM_015575.3:c.73A>G	NP_056390.2:p.Thr25Ala
NM_015575.4:c.73A>G	NP_056390.2:p.Thr25Ala
NR_103492.1:n.186A>G
ENST00000373563.8:c.73A>G	ENSP00000362664.4:p.Thr25Ala
ENST00000409196.7:c.73A>G	ENSP00000387070.3:p.Thr25Ala
ENST00000409451.7:c.73A>G	ENSP00000387170.3:p.Thr25Ala
ENST00000409480.5:c.73A>G	ENSP00000386765.1:p.Thr25Ala
ENST00000409547.5:c.73A>G	ENSP00000386537.1:p.Thr25Ala
ENST00000421433.5:c.73A>G	ENSP00000402053.1:p.Thr25Ala
ENST00000423659.5:c.73A>G	ENSP00000404195.1:p.Thr25Ala
ENST00000424038.1:c.73A>G	ENSP00000399064.1:p.Thr25Ala
ENST00000424038.2:c.73A>G	ENSP00000399064.1:p.Thr25Ala
ENST00000425040.5:c.73A>G	ENSP00000407161.1:p.Thr25Ala
ENST00000428883.5:c.73A>G	ENSP00000402712.1:p.Thr25Ala
ENST00000429187.5:c.73A>G	ENSP00000392991.1:p.Thr25Ala
ENST00000430720.5:c.73A>G	ENSP00000396958.1:p.Thr25Ala
ENST00000440945.5:c.73A>G	ENSP00000410297.1:p.Thr25Ala
ENST00000456491.5:c.73A>G	ENSP00000413612.1:p.Thr25Ala
ENST00000463554.5:n.225A>G
ENST00000629305.2:c.73A>G	ENSP00000487548.1:p.Thr25Ala