Canonical Allele Identifier: CA409105357
Gene: HNF4A HGNC NCBI

Linked Data

dbSNP Id: rs1298896114
MyVariant Identifiers: chr20:g.43042334C>G (hg19) chr20:g.44413694C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44413694C>G , CM000682.2:g.44413694C>G GRCh38
NC_000020.10:g.43042334C>G , CM000682.1:g.43042334C>G GRCh37
NC_000020.9:g.42475748C>G NCBI36
NG_009818.1:g.62894C>G , LRG_483:g.62894C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000316673.9:c.320C>G MANE Select ENSP00000315180.4:p.Ala107Gly
ENST00000316099.10:c.386C>G ENSP00000312987.3:p.Ala129Gly
ENST00000619550.5:c.360C>G
ENST00000683148.1:n.362C>G
ENST00000683657.1:n.1510C>G
ENST00000316099.9:c.386C>G ENSP00000312987.3:p.Ala129Gly
ENST00000316099.8:c.386C>G ENSP00000312987.3:p.Ala129Gly
ENST00000316673.8:c.320C>G ENSP00000315180.4:p.Ala107Gly
ENST00000372920.1:c.*153C>G ENSP00000362011.1:n.*153C>G
ENST00000415691.2:c.386C>G ENSP00000412111.1:p.Ala129Gly
ENST00000443598.6:c.386C>G ENSP00000410911.2:p.Ala129Gly
ENST00000457232.5:c.320C>G ENSP00000396216.1:p.Ala107Gly
ENST00000609795.5:c.320C>G ENSP00000476609.1:p.Ala107Gly
ENST00000619550.4:c.311C>G ENSP00000481331.1:p.Ala104Gly
NM_000457.4:c.386C>G , LRG_483t2:c.386C>G NP_000448.3:p.Ala129Gly
NM_001030003.2:c.320C>G NP_001025174.1:p.Ala107Gly
NM_001030004.2:c.320C>G NP_001025175.1:p.Ala107Gly
NM_001258355.1:c.365C>G NP_001245284.1:p.Ala122Gly
NM_001287182.1:c.311C>G NP_001274111.1:p.Ala104Gly
NM_001287183.1:c.311C>G , LRG_483t3:c.311C>G NP_001274112.1:p.Ala104Gly
NM_001287184.1:c.311C>G NP_001274113.1:p.Ala104Gly
NM_175914.4:c.320C>G , LRG_483t1:c.320C>G NP_787110.2:p.Ala107Gly
NM_178849.2:c.386C>G NP_849180.1:p.Ala129Gly
NM_178850.2:c.386C>G NP_849181.1:p.Ala129Gly
XM_005260407.2:c.503C>G XP_005260464.1:p.Ala168Gly
XM_011528797.1:c.434C>G XP_011527099.1:p.Ala145Gly
XM_011528798.1:c.434C>G XP_011527100.1:p.Ala145Gly
XM_005260407.4:c.503C>G XP_005260464.1:p.Ala168Gly
NM_001030003.3:c.320C>G NP_001025174.1:p.Ala107Gly
NM_001030004.3:c.320C>G NP_001025175.1:p.Ala107Gly
NM_001258355.2:c.365C>G NP_001245284.1:p.Ala122Gly
NM_001287182.2:c.311C>G NP_001274111.1:p.Ala104Gly
NM_001287184.2:c.311C>G NP_001274113.1:p.Ala104Gly
NM_178849.3:c.386C>G NP_849180.1:p.Ala129Gly
NM_178850.3:c.386C>G NP_849181.1:p.Ala129Gly
NM_000457.5:c.386C>G NP_000448.3:p.Ala129Gly
NM_000457.6:c.386C>G NP_000448.3:p.Ala129Gly
NM_001287183.2:c.311C>G NP_001274112.1:p.Ala104Gly
NM_175914.5:c.320C>G MANE Select NP_787110.2:p.Ala107Gly
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