Canonical Allele Identifier: CA351011394
Gene: GIGYF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232790875T>G , CM000664.2:g.232790875T>G GRCh38
NC_000002.11:g.233655585T>G , CM000664.1:g.233655585T>G GRCh37
NC_000002.10:g.233363829T>G NCBI36
NG_011847.1:g.98571T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373563.9:c.890T>G MANE Select ENSP00000362664.5:p.Met297Arg
ENST00000676848.1:c.236T>G ENSP00000503313.1:p.Met79Arg
ENST00000677450.1:c.371T>G ENSP00000503420.1:p.Met124Arg
ENST00000677591.1:c.146T>G ENSP00000503061.1:p.Met49Arg
ENST00000678230.1:c.383T>G ENSP00000504272.1:p.Met128Arg
ENST00000678339.1:c.146T>G ENSP00000503437.1:p.Met49Arg
ENST00000678466.1:c.146T>G ENSP00000504219.1:p.Met49Arg
ENST00000678885.1:c.146T>G ENSP00000503563.1:p.Met49Arg
ENST00000373563.8:c.890T>G ENSP00000362664.4:p.Met297Arg
ENST00000409196.7:c.872T>G ENSP00000387070.3:p.Met291Arg
ENST00000409451.7:c.956T>G ENSP00000387170.3:p.Met319Arg
ENST00000409480.5:c.956T>G ENSP00000386765.1:p.Met319Arg
ENST00000409547.5:c.890T>G ENSP00000386537.1:p.Met297Arg
ENST00000410033.1:c.236T>G ENSP00000387276.1:p.Met79Arg
ENST00000423659.5:c.719T>G ENSP00000404195.1:p.Met240Arg
ENST00000424414.6:c.146T>G ENSP00000401261.2:p.Met49Arg
ENST00000427649.5:c.146T>G ENSP00000398055.1:p.Met49Arg
ENST00000436349.5:c.146T>G ENSP00000400076.1:p.Met49Arg
ENST00000440945.5:c.872T>G ENSP00000410297.1:p.Met291Arg
ENST00000455139.5:c.146T>G ENSP00000395299.1:p.Met49Arg
ENST00000458528.1:c.107+129T>G ENSP00000389322.1:n.107+129T>G
ENST00000629305.2:c.956T>G ENSP00000487548.1:p.Met319Arg
NM_001103146.1:c.890T>G NP_001096616.1:p.Met297Arg
NM_001103147.1:c.956T>G NP_001096617.1:p.Met319Arg
NM_001103148.1:c.872T>G NP_001096618.1:p.Met291Arg
NM_015575.3:c.890T>G NP_056390.2:p.Met297Arg
NR_103492.1:n.1003T>G
NM_001103146.3:c.890T>G MANE Select NP_001096616.1:p.Met297Arg
NM_001103147.2:c.956T>G NP_001096617.1:p.Met319Arg
NM_001103148.2:c.872T>G NP_001096618.1:p.Met291Arg
NM_015575.4:c.890T>G NP_056390.2:p.Met297Arg