Canonical Allele Identifier: CA2531003115
Gene: HJV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.146019763del , CM000663.2:g.146019763del GRCh38
NC_000001.10:g.145415250del , CM000663.1:g.145415250del GRCh37
NC_000001.9:g.144126607del NCBI36
NG_011568.1:g.7060del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336751.11:c.98-29del MANE Select ENSP00000337014.5:n.98-29del
ENST00000636675.1:c.-58-29del ENSP00000490072.1:n.-58-29del
ENST00000336751.10:c.98-29del ENSP00000337014.5:n.98-29del
ENST00000357836.5:c.-242-29del ENSP00000350495.5:n.-242-29del
ENST00000421822.2:c.98-29del ENSP00000411863.2:n.98-29del
ENST00000475797.1:c.-21-1063del ENSP00000425716.1:n.-21-1063del
ENST00000497365.5:c.-58-29del ENSP00000421820.1:n.-58-29del
ENST00000634927.1:c.98-29del ENSP00000489347.1:n.98-29del
NM_001316767.1:c.-58-29del NP_001303696.1:n.-58-29del
NM_145277.4:c.-242-29del NP_660320.3:n.-242-29del
NM_202004.3:c.-58-29del NP_973733.1:n.-58-29del
NM_213652.3:c.-21-1063del NP_998817.1:n.-21-1063del
NM_213653.3:c.98-29del NP_998818.1:n.98-29del
XM_005272932.1:c.98-29del XP_005272989.1:n.98-29del
NM_001316767.2:c.-58-29del NP_001303696.1:n.-58-29del
NM_145277.5:c.-242-29del NP_660320.3:n.-242-29del
NM_202004.4:c.-58-29del NP_973733.1:n.-58-29del
NM_213652.4:c.-21-1063del NP_998817.1:n.-21-1063del
NM_001379352.1:c.98-29del NP_001366281.1:n.98-29del
NM_213653.4:c.98-29del MANE Select NP_998818.1:n.98-29del