Canonical Allele Identifier: CA766195792
Gene: GIGYF2 HGNC NCBI

Linked Data

dbSNP Id: rs1416971878

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232791669A>G , CM000664.2:g.232791669A>G GRCh38
NC_000002.11:g.233656379A>G , CM000664.1:g.233656379A>G GRCh37
NC_000002.10:g.233364623A>G NCBI36
NG_011847.1:g.99365A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373563.9:c.1282+223A>G MANE Select ENSP00000362664.5:n.1282+223A>G
ENST00000676848.1:c.628+223A>G ENSP00000503313.1:n.628+223A>G
ENST00000677450.1:c.763+223A>G ENSP00000503420.1:n.763+223A>G
ENST00000677591.1:c.538+223A>G ENSP00000503061.1:n.538+223A>G
ENST00000678230.1:c.775+223A>G ENSP00000504272.1:n.775+223A>G
ENST00000678339.1:c.538+223A>G ENSP00000503437.1:n.538+223A>G
ENST00000678466.1:c.538+223A>G ENSP00000504219.1:n.538+223A>G
ENST00000678885.1:c.538+223A>G ENSP00000503563.1:n.538+223A>G
ENST00000373563.8:c.1282+223A>G ENSP00000362664.4:n.1282+223A>G
ENST00000409196.7:c.1264+223A>G ENSP00000387070.3:n.1264+223A>G
ENST00000409451.7:c.1345+223A>G ENSP00000387170.3:n.1345+223A>G
ENST00000409480.5:c.1348+223A>G ENSP00000386765.1:n.1348+223A>G
ENST00000409547.5:c.1282+223A>G ENSP00000386537.1:n.1282+223A>G
ENST00000423659.5:c.1111+223A>G ENSP00000404195.1:n.1111+223A>G
ENST00000440945.5:c.1264+223A>G ENSP00000410297.1:n.1264+223A>G
ENST00000458528.1:c.*275+223A>G ENSP00000389322.1:n.*275+223A>G
ENST00000629305.2:c.1348+223A>G ENSP00000487548.1:n.1348+223A>G
NM_001103146.1:c.1282+223A>G NP_001096616.1:n.1282+223A>G
NM_001103147.1:c.1345+223A>G NP_001096617.1:n.1345+223A>G
NM_001103148.1:c.1264+223A>G NP_001096618.1:n.1264+223A>G
NM_015575.3:c.1282+223A>G NP_056390.2:n.1282+223A>G
NR_103492.1:n.1395+223A>G
NM_001103146.3:c.1282+223A>G MANE Select NP_001096616.1:n.1282+223A>G
NM_001103147.2:c.1345+223A>G NP_001096617.1:n.1345+223A>G
NM_001103148.2:c.1264+223A>G NP_001096618.1:n.1264+223A>G
NM_015575.4:c.1282+223A>G NP_056390.2:n.1282+223A>G