Canonical Allele Identifier: CA351011535

Gene: GIGYF2

Linked Data

• MyVariant Identifiers: chr2:g.233655626G>C (hg19) ; chr2:g.232790916G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232790916G>C , CM000664.2:g.232790916G>C	GRCh38
NC_000002.11:g.233655626G>C , CM000664.1:g.233655626G>C	GRCh37
NC_000002.10:g.233363870G>C	NCBI36
NG_011847.1:g.98612G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373563.9:c.930+1G>C MANE Select	ENSP00000362664.5:n.930+1G>C
ENST00000676848.1:c.276+1G>C	ENSP00000503313.1:n.276+1G>C
ENST00000677450.1:c.411+1G>C	ENSP00000503420.1:n.411+1G>C
ENST00000677591.1:c.186+1G>C	ENSP00000503061.1:n.186+1G>C
ENST00000678230.1:c.423+1G>C	ENSP00000504272.1:n.423+1G>C
ENST00000678339.1:c.186+1G>C	ENSP00000503437.1:n.186+1G>C
ENST00000678466.1:c.186+1G>C	ENSP00000504219.1:n.186+1G>C
ENST00000678885.1:c.186+1G>C	ENSP00000503563.1:n.186+1G>C
ENST00000373563.8:c.930+1G>C	ENSP00000362664.4:n.930+1G>C
ENST00000409196.7:c.912+1G>C	ENSP00000387070.3:n.912+1G>C
ENST00000409451.7:c.996+1G>C	ENSP00000387170.3:n.996+1G>C
ENST00000409480.5:c.996+1G>C	ENSP00000386765.1:n.996+1G>C
ENST00000409547.5:c.930+1G>C	ENSP00000386537.1:n.930+1G>C
ENST00000410033.1:c.276+1G>C	ENSP00000387276.1:n.276+1G>C
ENST00000423659.5:c.759+1G>C	ENSP00000404195.1:n.759+1G>C
ENST00000424414.6:c.186+1G>C	ENSP00000401261.2:n.186+1G>C
ENST00000427649.5:c.186+1G>C	ENSP00000398055.1:n.186+1G>C
ENST00000440945.5:c.912+1G>C	ENSP00000410297.1:n.912+1G>C
ENST00000458528.1:c.108-96G>C	ENSP00000389322.1:n.108-96G>C
ENST00000629305.2:c.996+1G>C	ENSP00000487548.1:n.996+1G>C
NM_001103146.1:c.930+1G>C	NP_001096616.1:n.930+1G>C
NM_001103147.1:c.996+1G>C	NP_001096617.1:n.996+1G>C
NM_001103148.1:c.912+1G>C	NP_001096618.1:n.912+1G>C
NM_015575.3:c.930+1G>C	NP_056390.2:n.930+1G>C
NR_103492.1:n.1043+1G>C
NM_001103146.3:c.930+1G>C MANE Select	NP_001096616.1:n.930+1G>C
NM_001103147.2:c.996+1G>C	NP_001096617.1:n.996+1G>C
NM_001103148.2:c.912+1G>C	NP_001096618.1:n.912+1G>C
NM_015575.4:c.930+1G>C	NP_056390.2:n.930+1G>C