Canonical Allele Identifier: CA2652972308

Gene: HNF4A

Linked Data

• gnomAD v4: 20-44413605-TCCTGCTCCCACTCCTCATCAGTCACAGACACCCCCACCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44413609_44413647del , CM000682.2:g.44413609_44413647del	GRCh38
NC_000020.10:g.43042249_43042287del , CM000682.1:g.43042249_43042287del	GRCh37
NC_000020.9:g.42475663_42475701del	NCBI36
NG_009818.1:g.62809_62847del , LRG_483:g.62809_62847del

Transcript Alleles

HGVS	Amino-acid change
ENST00000316673.9:c.320-85_320-47del MANE Select	ENSP00000315180.4:n.320-85_320-47del
ENST00000316099.10:c.386-85_386-47del	ENSP00000312987.3:n.386-85_386-47del
ENST00000619550.5:c.360-85_360-47del
ENST00000683148.1:n.362-85_362-47del
ENST00000683657.1:n.1510-85_1510-47del
ENST00000316099.9:c.386-85_386-47del	ENSP00000312987.3:n.386-85_386-47del
ENST00000316099.8:c.386-85_386-47del	ENSP00000312987.3:n.386-85_386-47del
ENST00000316673.8:c.320-85_320-47del	ENSP00000315180.4:n.320-85_320-47del
ENST00000372920.1:c.*153-85_*153-47del	ENSP00000362011.1:n.*153-85_*153-47del
ENST00000415691.2:c.386-85_386-47del	ENSP00000412111.1:n.386-85_386-47del
ENST00000443598.6:c.386-85_386-47del	ENSP00000410911.2:n.386-85_386-47del
ENST00000457232.5:c.320-85_320-47del	ENSP00000396216.1:n.320-85_320-47del
ENST00000609795.5:c.320-85_320-47del	ENSP00000476609.1:n.320-85_320-47del
ENST00000619550.4:c.311-85_311-47del	ENSP00000481331.1:n.311-85_311-47del
NM_000457.4:c.386-85_386-47del , LRG_483t2:c.386-85_386-47del	NP_000448.3:n.386-85_386-47del
NM_001030003.2:c.320-85_320-47del	NP_001025174.1:n.320-85_320-47del
NM_001030004.2:c.320-85_320-47del	NP_001025175.1:n.320-85_320-47del
NM_001258355.1:c.365-85_365-47del	NP_001245284.1:n.365-85_365-47del
NM_001287182.1:c.311-85_311-47del	NP_001274111.1:n.311-85_311-47del
NM_001287183.1:c.311-85_311-47del , LRG_483t3:c.311-85_311-47del	NP_001274112.1:n.311-85_311-47del
NM_001287184.1:c.311-85_311-47del	NP_001274113.1:n.311-85_311-47del
NM_175914.4:c.320-85_320-47del , LRG_483t1:c.320-85_320-47del	NP_787110.2:n.320-85_320-47del
NM_178849.2:c.386-85_386-47del	NP_849180.1:n.386-85_386-47del
NM_178850.2:c.386-85_386-47del	NP_849181.1:n.386-85_386-47del
XM_005260407.2:c.503-85_503-47del	XP_005260464.1:n.503-85_503-47del
XM_011528797.1:c.434-85_434-47del	XP_011527099.1:n.434-85_434-47del
XM_011528798.1:c.434-85_434-47del	XP_011527100.1:n.434-85_434-47del
XM_005260407.4:c.503-85_503-47del	XP_005260464.1:n.503-85_503-47del
NM_001030003.3:c.320-85_320-47del	NP_001025174.1:n.320-85_320-47del
NM_001030004.3:c.320-85_320-47del	NP_001025175.1:n.320-85_320-47del
NM_001258355.2:c.365-85_365-47del	NP_001245284.1:n.365-85_365-47del
NM_001287182.2:c.311-85_311-47del	NP_001274111.1:n.311-85_311-47del
NM_001287184.2:c.311-85_311-47del	NP_001274113.1:n.311-85_311-47del
NM_178849.3:c.386-85_386-47del	NP_849180.1:n.386-85_386-47del
NM_178850.3:c.386-85_386-47del	NP_849181.1:n.386-85_386-47del
NM_000457.5:c.386-85_386-47del	NP_000448.3:n.386-85_386-47del
NM_000457.6:c.386-85_386-47del	NP_000448.3:n.386-85_386-47del
NM_001287183.2:c.311-85_311-47del	NP_001274112.1:n.311-85_311-47del
NM_175914.5:c.320-85_320-47del MANE Select	NP_787110.2:n.320-85_320-47del