Canonical Allele Identifier: CA2574047893
Gene: HJV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.146018395del , CM000663.2:g.146018395del GRCh38
NC_000001.10:g.145416620del , CM000663.1:g.145416620del GRCh37
NC_000001.9:g.144127977del NCBI36
NG_011568.1:g.8430del

Transcript Alleles

HGVS Amino-acid change
ENST00000336751.11:c.965del MANE Select ENSP00000337014.5:p.Pro322LeufsTer17
ENST00000636675.1:c.287del ENSP00000490072.1:p.Pro96LeufsTer17
ENST00000336751.10:c.965del ENSP00000337014.5:p.Pro322LeufsTer17
ENST00000357836.5:c.626del ENSP00000350495.5:p.Pro209LeufsTer17
ENST00000475797.1:c.287del ENSP00000425716.1:p.Pro96LeufsTer17
ENST00000497365.5:c.287del ENSP00000421820.1:p.Pro96LeufsTer17
NM_001316767.1:c.287del NP_001303696.1:p.Pro96LeufsTer17
NM_145277.4:c.626del NP_660320.3:p.Pro209LeufsTer17
NM_202004.3:c.287del NP_973733.1:p.Pro96LeufsTer17
NM_213652.3:c.287del NP_998817.1:p.Pro96LeufsTer17
NM_213653.3:c.965del NP_998818.1:p.Pro322LeufsTer17
XM_005272932.1:c.965del XP_005272989.1:p.Pro322LeufsTer17
NM_001316767.2:c.287del NP_001303696.1:p.Pro96LeufsTer17
NM_145277.5:c.626del NP_660320.3:p.Pro209LeufsTer17
NM_202004.4:c.287del NP_973733.1:p.Pro96LeufsTer17
NM_213652.4:c.287del NP_998817.1:p.Pro96LeufsTer17
NM_001379352.1:c.965del NP_001366281.1:p.Pro322LeufsTer17
NM_213653.4:c.965del MANE Select NP_998818.1:p.Pro322LeufsTer17