Canonical Allele Identifier: CA2687684216

Gene: HNF4G

Linked Data

• gnomAD v4: 8-75566443-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.75566443T>A , CM000670.2:g.75566443T>A	GRCh38
NC_000008.10:g.76478678T>A , CM000670.1:g.76478678T>A	GRCh37
NC_000008.9:g.76641233T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000396423.4:c.*2347T>A MANE Select	ENSP00000379701.3:n.*2347T>A
ENST00000674002.1:c.*2347T>A	ENSP00000501146.1:n.*2347T>A
ENST00000396423.2:c.*2347T>A	ENSP00000379701.2:n.*2347T>A
NM_004133.4:c.*2347T>A	NP_004124.4:n.*2347T>A
XM_011517514.1:c.*2347T>A	XP_011515816.1:n.*2347T>A
XM_011517515.1:c.*2347T>A	XP_011515817.1:n.*2347T>A
XM_011517516.1:c.*2347T>A	XP_011515818.1:n.*2347T>A
XM_011517517.1:c.*2347T>A	XP_011515819.1:n.*2347T>A
XM_011517518.1:c.*2347T>A	XP_011515820.1:n.*2347T>A
XM_011517519.1:c.*2347T>A	XP_011515821.1:n.*2347T>A
XM_011517520.1:c.*2347T>A	XP_011515822.1:n.*2347T>A
NM_001330561.1:c.*2347T>A	NP_001317490.1:n.*2347T>A
NM_001330561.2:c.*2347T>A	NP_001317490.1:n.*2347T>A
NM_004133.5:c.*2347T>A MANE Select	NP_004124.5:n.*2347T>A