Canonical Allele Identifier: CA1198821698
Gene: HJV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.146020140C= , CM000663.2:g.146020140C= GRCh38
NC_000001.10:g.145414873G= , CM000663.1:g.145414873G= GRCh37
NC_000001.9:g.144126230G= NCBI36
NG_011568.1:g.6683G=

Transcript Alleles

HGVS Amino-acid change
ENST00000336751.11:c.92G= MANE Select ENSP00000337014.5:p.Gly31=
ENST00000636675.1:c.-58-406G= ENSP00000490072.1:n.-58-406G=
ENST00000336751.10:c.92G= ENSP00000337014.5:p.Gly31=
ENST00000357836.5:c.-242-406G= ENSP00000350495.5:n.-242-406G=
ENST00000421822.2:c.92G= ENSP00000411863.2:p.Gly31=
ENST00000475797.1:c.-21-1440G= ENSP00000425716.1:n.-21-1440G=
ENST00000497365.5:c.-58-406G= ENSP00000421820.1:n.-58-406G=
ENST00000634927.1:c.92G= ENSP00000489347.1:p.Gly31=
NM_001316767.1:c.-64G= NP_001303696.1:n.-64G=
NM_145277.4:c.-242-406G= NP_660320.3:n.-242-406G=
NM_202004.3:c.-58-406G= NP_973733.1:n.-58-406G=
NM_213652.3:c.-21-1440G= NP_998817.1:n.-21-1440G=
NM_213653.3:c.92G= NP_998818.1:p.Gly31=
XM_005272932.1:c.92G= XP_005272989.1:p.Gly31=
NM_001316767.2:c.-64G= NP_001303696.1:n.-64G=
NM_145277.5:c.-242-406G= NP_660320.3:n.-242-406G=
NM_202004.4:c.-58-406G= NP_973733.1:n.-58-406G=
NM_213652.4:c.-21-1440G= NP_998817.1:n.-21-1440G=
NM_001379352.1:c.92G= NP_001366281.1:p.Gly31=
NM_213653.4:c.92G= MANE Select NP_998818.1:p.Gly31=