Canonical Allele Identifier: CA2663643231

Gene: GIGYF2

Linked Data

• gnomAD v4: 2-232791475-A-AGGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232791475_232791476insGGCC , CM000664.2:g.232791475_232791476insGGCC	GRCh38
NC_000002.11:g.233656185_233656186insGGCC , CM000664.1:g.233656185_233656186insGGCC	GRCh37
NC_000002.10:g.233364429_233364430insGGCC	NCBI36
NG_011847.1:g.99171_99172insGGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373563.9:c.1282+29_1282+30insGGCC MANE Select	ENSP00000362664.5:n.1282+29_1282+30insGGCC
ENST00000676848.1:c.628+29_628+30insGGCC	ENSP00000503313.1:n.628+29_628+30insGGCC
ENST00000677450.1:c.763+29_763+30insGGCC	ENSP00000503420.1:n.763+29_763+30insGGCC
ENST00000677591.1:c.538+29_538+30insGGCC	ENSP00000503061.1:n.538+29_538+30insGGCC
ENST00000678230.1:c.775+29_775+30insGGCC	ENSP00000504272.1:n.775+29_775+30insGGCC
ENST00000678339.1:c.538+29_538+30insGGCC	ENSP00000503437.1:n.538+29_538+30insGGCC
ENST00000678466.1:c.538+29_538+30insGGCC	ENSP00000504219.1:n.538+29_538+30insGGCC
ENST00000678885.1:c.538+29_538+30insGGCC	ENSP00000503563.1:n.538+29_538+30insGGCC
ENST00000373563.8:c.1282+29_1282+30insGGCC	ENSP00000362664.4:n.1282+29_1282+30insGGCC
ENST00000409196.7:c.1264+29_1264+30insGGCC	ENSP00000387070.3:n.1264+29_1264+30insGGCC
ENST00000409451.7:c.1345+29_1345+30insGGCC	ENSP00000387170.3:n.1345+29_1345+30insGGCC
ENST00000409480.5:c.1348+29_1348+30insGGCC	ENSP00000386765.1:n.1348+29_1348+30insGGCC
ENST00000409547.5:c.1282+29_1282+30insGGCC	ENSP00000386537.1:n.1282+29_1282+30insGGCC
ENST00000423659.5:c.1111+29_1111+30insGGCC	ENSP00000404195.1:n.1111+29_1111+30insGGCC
ENST00000440945.5:c.1264+29_1264+30insGGCC	ENSP00000410297.1:n.1264+29_1264+30insGGCC
ENST00000458528.1:c.*275+29_*275+30insGGCC	ENSP00000389322.1:n.*275+29_*275+30insGGCC
ENST00000629305.2:c.1348+29_1348+30insGGCC	ENSP00000487548.1:n.1348+29_1348+30insGGCC
NM_001103146.1:c.1282+29_1282+30insGGCC	NP_001096616.1:n.1282+29_1282+30insGGCC
NM_001103147.1:c.1345+29_1345+30insGGCC	NP_001096617.1:n.1345+29_1345+30insGGCC
NM_001103148.1:c.1264+29_1264+30insGGCC	NP_001096618.1:n.1264+29_1264+30insGGCC
NM_015575.3:c.1282+29_1282+30insGGCC	NP_056390.2:n.1282+29_1282+30insGGCC
NR_103492.1:n.1395+29_1395+30insGGCC
NM_001103146.3:c.1282+29_1282+30insGGCC MANE Select	NP_001096616.1:n.1282+29_1282+30insGGCC
NM_001103147.2:c.1345+29_1345+30insGGCC	NP_001096617.1:n.1345+29_1345+30insGGCC
NM_001103148.2:c.1264+29_1264+30insGGCC	NP_001096618.1:n.1264+29_1264+30insGGCC
NM_015575.4:c.1282+29_1282+30insGGCC	NP_056390.2:n.1282+29_1282+30insGGCC