Canonical Allele Identifier: CA855353776

Gene: HNF4G

Linked Data

• dbSNP Id: rs1227551328
• MyVariant Identifiers: chr8:g.76478673_76478674del (hg19) ; chr8:g.75566438_75566439del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.75566441_75566442del , CM000670.2:g.75566441_75566442del	GRCh38
NC_000008.10:g.76478676_76478677del , CM000670.1:g.76478676_76478677del	GRCh37
NC_000008.9:g.76641231_76641232del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396423.4:c.*2345_*2346del MANE Select	ENSP00000379701.3:n.*2345_*2346del
ENST00000674002.1:c.*2345_*2346del	ENSP00000501146.1:n.*2345_*2346del
ENST00000396423.2:c.*2345_*2346del	ENSP00000379701.2:n.*2345_*2346del
NM_004133.4:c.*2345_*2346del	NP_004124.4:n.*2345_*2346del
XM_011517514.1:c.*2345_*2346del	XP_011515816.1:n.*2345_*2346del
XM_011517515.1:c.*2345_*2346del	XP_011515817.1:n.*2345_*2346del
XM_011517516.1:c.*2345_*2346del	XP_011515818.1:n.*2345_*2346del
XM_011517517.1:c.*2345_*2346del	XP_011515819.1:n.*2345_*2346del
XM_011517518.1:c.*2345_*2346del	XP_011515820.1:n.*2345_*2346del
XM_011517519.1:c.*2345_*2346del	XP_011515821.1:n.*2345_*2346del
XM_011517520.1:c.*2345_*2346del	XP_011515822.1:n.*2345_*2346del
NM_001330561.1:c.*2345_*2346del	NP_001317490.1:n.*2345_*2346del
NM_001330561.2:c.*2345_*2346del	NP_001317490.1:n.*2345_*2346del
NM_004133.5:c.*2345_*2346del MANE Select	NP_004124.5:n.*2345_*2346del