Canonical Allele Identifier: CA1335433644

Gene: GIGYF2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232791587_232791591delinsCCAGT , CM000664.2:g.232791587_232791591delinsCCAGT	GRCh38
NC_000002.11:g.233656297_233656301delinsCCAGT , CM000664.1:g.233656297_233656301delinsCCAGT	GRCh37
NC_000002.10:g.233364541_233364545delinsCCAGT	NCBI36
NG_011847.1:g.99283_99287delinsCCAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373563.9:c.1282+141_1282+145delinsCCAGT MANE Select	ENSP00000362664.5:n.1282+141_1282+145delinsCCAGT
ENST00000676848.1:c.628+141_628+145delinsCCAGT	ENSP00000503313.1:n.628+141_628+145delinsCCAGT
ENST00000677450.1:c.763+141_763+145delinsCCAGT	ENSP00000503420.1:n.763+141_763+145delinsCCAGT
ENST00000677591.1:c.538+141_538+145delinsCCAGT	ENSP00000503061.1:n.538+141_538+145delinsCCAGT
ENST00000678230.1:c.775+141_775+145delinsCCAGT	ENSP00000504272.1:n.775+141_775+145delinsCCAGT
ENST00000678339.1:c.538+141_538+145delinsCCAGT	ENSP00000503437.1:n.538+141_538+145delinsCCAGT
ENST00000678466.1:c.538+141_538+145delinsCCAGT	ENSP00000504219.1:n.538+141_538+145delinsCCAGT
ENST00000678885.1:c.538+141_538+145delinsCCAGT	ENSP00000503563.1:n.538+141_538+145delinsCCAGT
ENST00000373563.8:c.1282+141_1282+145delinsCCAGT	ENSP00000362664.4:n.1282+141_1282+145delinsCCAGT
ENST00000409196.7:c.1264+141_1264+145delinsCCAGT	ENSP00000387070.3:n.1264+141_1264+145delinsCCAGT
ENST00000409451.7:c.1345+141_1345+145delinsCCAGT	ENSP00000387170.3:n.1345+141_1345+145delinsCCAGT
ENST00000409480.5:c.1348+141_1348+145delinsCCAGT	ENSP00000386765.1:n.1348+141_1348+145delinsCCAGT
ENST00000409547.5:c.1282+141_1282+145delinsCCAGT	ENSP00000386537.1:n.1282+141_1282+145delinsCCAGT
ENST00000423659.5:c.1111+141_1111+145delinsCCAGT	ENSP00000404195.1:n.1111+141_1111+145delinsCCAGT
ENST00000440945.5:c.1264+141_1264+145delinsCCAGT	ENSP00000410297.1:n.1264+141_1264+145delinsCCAGT
ENST00000458528.1:c.*275+141_*275+145delinsCCAGT	ENSP00000389322.1:n.*275+141_*275+145delinsCCAGT
ENST00000629305.2:c.1348+141_1348+145delinsCCAGT	ENSP00000487548.1:n.1348+141_1348+145delinsCCAGT
NM_001103146.1:c.1282+141_1282+145delinsCCAGT	NP_001096616.1:n.1282+141_1282+145delinsCCAGT
NM_001103147.1:c.1345+141_1345+145delinsCCAGT	NP_001096617.1:n.1345+141_1345+145delinsCCAGT
NM_001103148.1:c.1264+141_1264+145delinsCCAGT	NP_001096618.1:n.1264+141_1264+145delinsCCAGT
NM_015575.3:c.1282+141_1282+145delinsCCAGT	NP_056390.2:n.1282+141_1282+145delinsCCAGT
NR_103492.1:n.1395+141_1395+145delinsCCAGT
NM_001103146.3:c.1282+141_1282+145delinsCCAGT MANE Select	NP_001096616.1:n.1282+141_1282+145delinsCCAGT
NM_001103147.2:c.1345+141_1345+145delinsCCAGT	NP_001096617.1:n.1345+141_1345+145delinsCCAGT
NM_001103148.2:c.1264+141_1264+145delinsCCAGT	NP_001096618.1:n.1264+141_1264+145delinsCCAGT
NM_015575.4:c.1282+141_1282+145delinsCCAGT	NP_056390.2:n.1282+141_1282+145delinsCCAGT