Canonical Allele Identifier: CA342134106
Gene: HJV HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.146018311T>G , CM000663.2:g.146018311T>G GRCh38
NC_000001.10:g.145416702A>C , CM000663.1:g.145416702A>C GRCh37
NC_000001.9:g.144128059A>C NCBI36
NG_011568.1:g.8512A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000336751.11:c.1047A>C MANE Select ENSP00000337014.5:p.Glu349Asp
ENST00000636675.1:c.369A>C ENSP00000490072.1:p.Glu123Asp
ENST00000336751.10:c.1047A>C ENSP00000337014.5:p.Glu349Asp
ENST00000357836.5:c.708A>C ENSP00000350495.5:p.Glu236Asp
ENST00000475797.1:c.369A>C ENSP00000425716.1:p.Glu123Asp
ENST00000497365.5:c.369A>C ENSP00000421820.1:p.Glu123Asp
NM_001316767.1:c.369A>C NP_001303696.1:p.Glu123Asp
NM_145277.4:c.708A>C NP_660320.3:p.Glu236Asp
NM_202004.3:c.369A>C NP_973733.1:p.Glu123Asp
NM_213652.3:c.369A>C NP_998817.1:p.Glu123Asp
NM_213653.3:c.1047A>C NP_998818.1:p.Glu349Asp
XM_005272932.1:c.1047A>C XP_005272989.1:p.Glu349Asp
NM_001316767.2:c.369A>C NP_001303696.1:p.Glu123Asp
NM_145277.5:c.708A>C NP_660320.3:p.Glu236Asp
NM_202004.4:c.369A>C NP_973733.1:p.Glu123Asp
NM_213652.4:c.369A>C NP_998817.1:p.Glu123Asp
NM_001379352.1:c.1047A>C NP_001366281.1:p.Glu349Asp
NM_213653.4:c.1047A>C MANE Select NP_998818.1:p.Glu349Asp