Canonical Allele Identifier: CA2647575837
Gene: HJV HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.146019455del , CM000663.2:g.146019455del GRCh38
NC_000001.10:g.145415561del , CM000663.1:g.145415561del GRCh37
NC_000001.9:g.144126918del NCBI36
NG_011568.1:g.7371del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336751.11:c.380del MANE Select ENSP00000337014.5:p.Pro127LeufsTer?
ENST00000636675.1:c.-22+246del ENSP00000490072.1:n.-22+246del
ENST00000336751.10:c.380del ENSP00000337014.5:p.Pro127LeufsTer?
ENST00000357836.5:c.41del ENSP00000350495.5:p.Pro14LeufsTer?
ENST00000475797.1:c.-21-752del ENSP00000425716.1:n.-21-752del
ENST00000497365.5:c.-22+246del ENSP00000421820.1:n.-22+246del
ENST00000634927.1:c.134+246del ENSP00000489347.1:n.134+246del
NM_001316767.1:c.-22+246del NP_001303696.1:n.-22+246del
NM_145277.4:c.41del NP_660320.3:p.Pro14LeufsTer?
NM_202004.3:c.-22+246del NP_973733.1:n.-22+246del
NM_213652.3:c.-21-752del NP_998817.1:n.-21-752del
NM_213653.3:c.380del NP_998818.1:p.Pro127LeufsTer?
XM_005272932.1:c.380del XP_005272989.1:p.Pro127LeufsTer?
NM_001316767.2:c.-22+246del NP_001303696.1:n.-22+246del
NM_145277.5:c.41del NP_660320.3:p.Pro14LeufsTer?
NM_202004.4:c.-22+246del NP_973733.1:n.-22+246del
NM_213652.4:c.-21-752del NP_998817.1:n.-21-752del
NM_001379352.1:c.380del NP_001366281.1:p.Pro127LeufsTer?
NM_213653.4:c.380del MANE Select NP_998818.1:p.Pro127LeufsTer?