Canonical Allele Identifier: CA9870418
Gene: HNF4A HGNC NCBI

Linked Data

dbSNP Id: rs759229384

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44424149_44424150insGGGGAGCCTATTCTAACACAGTAGAAG , CM000682.2:g.44424149_44424150insGGGGAGCCTATTCTAACACAGTAGAAG GRCh38
NC_000020.10:g.43052789_43052790insGGGGAGCCTATTCTAACACAGTAGAAG , CM000682.1:g.43052789_43052790insGGGGAGCCTATTCTAACACAGTAGAAG GRCh37
NC_000020.9:g.42486203_42486204insGGGGAGCCTATTCTAACACAGTAGAAG NCBI36
NG_009818.1:g.73349_73350insGGGGAGCCTATTCTAACACAGTAGAAG , LRG_483:g.73349_73350insGGGGAGCCTATTCTAACACAGTAGAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000316673.9:c.958_959insGGGGAGCCTATTCTAACACAGTAGAAG MANE Select ENSP00000315180.4:p.Pro320delinsArgGlyAla...
ENST00000316099.10:c.1024_1025insGGGGAGCCTATTCTAACACAGTAGAAG ENSP00000312987.3:p.Pro342delinsArgGlyAla...
ENST00000619550.5:c.998_999insGGGGAGCCTATTCTAACACAGTAGAAG
ENST00000316099.9:c.1024_1025insGGGGAGCCTATTCTAACACAGTAGAAG ENSP00000312987.3:p.Pro342delinsArgGlyAla...
ENST00000316099.8:c.1024_1025insGGGGAGCCTATTCTAACACAGTAGAAG ENSP00000312987.3:p.Pro342delinsArgGlyAla...
ENST00000316673.8:c.958_959insGGGGAGCCTATTCTAACACAGTAGAAG ENSP00000315180.4:p.Pro320delinsArgGlyAla...
ENST00000372920.1:c.*791_*792insGGGGAGCCTATTCTAACACAGTAGAAG ENSP00000362011.1:n.*791_*792insGGGGAGCCT...
ENST00000415691.2:c.1024_1025insGGGGAGCCTATTCTAACACAGTAGAAG ENSP00000412111.1:p.Pro342delinsArgGlyAla...
ENST00000443598.6:c.1024_1025insGGGGAGCCTATTCTAACACAGTAGAAG ENSP00000410911.2:p.Pro342delinsArgGlyAla...
ENST00000457232.5:c.958_959insGGGGAGCCTATTCTAACACAGTAGAAG ENSP00000396216.1:p.Pro320delinsArgGlyAla...
ENST00000609795.5:c.958_959insGGGGAGCCTATTCTAACACAGTAGAAG ENSP00000476609.1:p.Pro320delinsArgGlyAla...
ENST00000619550.4:c.949_950insGGGGAGCCTATTCTAACACAGTAGAAG ENSP00000481331.1:p.Pro317delinsArgGlyAla...
NM_000457.4:c.1024_1025insGGGGAGCCTATTCTAACACAGTAGAAG , LRG_483t2:c.1024_1025insGGGGAGCCTATTCTAACACAGTAGAAG NP_000448.3:p.Pro342delinsArgGlyAlaTyrSer...
NM_001030003.2:c.958_959insGGGGAGCCTATTCTAACACAGTAGAAG NP_001025174.1:p.Pro320delinsArgGlyAlaTyr...
NM_001030004.2:c.958_959insGGGGAGCCTATTCTAACACAGTAGAAG NP_001025175.1:p.Pro320delinsArgGlyAlaTyr...
NM_001258355.1:c.1003_1004insGGGGAGCCTATTCTAACACAGTAGAAG NP_001245284.1:p.Pro335delinsArgGlyAlaTyr...
NM_001287182.1:c.949_950insGGGGAGCCTATTCTAACACAGTAGAAG NP_001274111.1:p.Pro317delinsArgGlyAlaTyr...
NM_001287183.1:c.949_950insGGGGAGCCTATTCTAACACAGTAGAAG , LRG_483t3:c.949_950insGGGGAGCCTATTCTAACACAGTAGAAG NP_001274112.1:p.Pro317delinsArgGlyAlaTyr...
NM_001287184.1:c.949_950insGGGGAGCCTATTCTAACACAGTAGAAG NP_001274113.1:p.Pro317delinsArgGlyAlaTyr...
NM_175914.4:c.958_959insGGGGAGCCTATTCTAACACAGTAGAAG , LRG_483t1:c.958_959insGGGGAGCCTATTCTAACACAGTAGAAG NP_787110.2:p.Pro320delinsArgGlyAlaTyrSer...
NM_178849.2:c.1024_1025insGGGGAGCCTATTCTAACACAGTAGAAG NP_849180.1:p.Pro342delinsArgGlyAlaTyrSer...
NM_178850.2:c.1024_1025insGGGGAGCCTATTCTAACACAGTAGAAG NP_849181.1:p.Pro342delinsArgGlyAlaTyrSer...
XM_005260407.2:c.1141_1142insGGGGAGCCTATTCTAACACAGTAGAAG XP_005260464.1:p.Pro381delinsArgGlyAlaTyr...
XM_011528797.1:c.1072_1073insGGGGAGCCTATTCTAACACAGTAGAAG XP_011527099.1:p.Pro358delinsArgGlyAlaTyr...
XM_011528798.1:c.1072_1073insGGGGAGCCTATTCTAACACAGTAGAAG XP_011527100.1:p.Pro358delinsArgGlyAlaTyr...
XM_005260407.4:c.1141_1142insGGGGAGCCTATTCTAACACAGTAGAAG XP_005260464.1:p.Pro381delinsArgGlyAlaTyr...
NM_001030003.3:c.958_959insGGGGAGCCTATTCTAACACAGTAGAAG NP_001025174.1:p.Pro320delinsArgGlyAlaTyr...
NM_001030004.3:c.958_959insGGGGAGCCTATTCTAACACAGTAGAAG NP_001025175.1:p.Pro320delinsArgGlyAlaTyr...
NM_001258355.2:c.1003_1004insGGGGAGCCTATTCTAACACAGTAGAAG NP_001245284.1:p.Pro335delinsArgGlyAlaTyr...
NM_001287182.2:c.949_950insGGGGAGCCTATTCTAACACAGTAGAAG NP_001274111.1:p.Pro317delinsArgGlyAlaTyr...
NM_001287184.2:c.949_950insGGGGAGCCTATTCTAACACAGTAGAAG NP_001274113.1:p.Pro317delinsArgGlyAlaTyr...
NM_178849.3:c.1024_1025insGGGGAGCCTATTCTAACACAGTAGAAG NP_849180.1:p.Pro342delinsArgGlyAlaTyrSer...
NM_178850.3:c.1024_1025insGGGGAGCCTATTCTAACACAGTAGAAG NP_849181.1:p.Pro342delinsArgGlyAlaTyrSer...
NM_000457.5:c.1024_1025insGGGGAGCCTATTCTAACACAGTAGAAG NP_000448.3:p.Pro342delinsArgGlyAlaTyrSer...
NM_000457.6:c.1024_1025insGGGGAGCCTATTCTAACACAGTAGAAG NP_000448.3:p.Pro342delinsArgGlyAlaTyrSer...
NM_001287183.2:c.949_950insGGGGAGCCTATTCTAACACAGTAGAAG NP_001274112.1:p.Pro317delinsArgGlyAlaTyr...
NM_175914.5:c.958_959insGGGGAGCCTATTCTAACACAGTAGAAG MANE Select NP_787110.2:p.Pro320delinsArgGlyAlaTyrSer...