Canonical Allele Identifier: CA1198821400
Gene: HJV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.146019501C= , CM000663.2:g.146019501C= GRCh38
NC_000001.10:g.145415512G= , CM000663.1:g.145415512G= GRCh37
NC_000001.9:g.144126869G= NCBI36
NG_011568.1:g.7322G=

Transcript Alleles

HGVS Amino-acid change
ENST00000336751.11:c.331G= MANE Select ENSP00000337014.5:p.Glu111=
ENST00000636675.1:c.-22+197G= ENSP00000490072.1:n.-22+197G=
ENST00000336751.10:c.331G= ENSP00000337014.5:p.Glu111=
ENST00000357836.5:c.-9G= ENSP00000350495.5:n.-9G=
ENST00000475797.1:c.-21-801G= ENSP00000425716.1:n.-21-801G=
ENST00000497365.5:c.-22+197G= ENSP00000421820.1:n.-22+197G=
ENST00000634927.1:c.134+197G= ENSP00000489347.1:n.134+197G=
NM_001316767.1:c.-22+197G= NP_001303696.1:n.-22+197G=
NM_145277.4:c.-9G= NP_660320.3:n.-9G=
NM_202004.3:c.-22+197G= NP_973733.1:n.-22+197G=
NM_213652.3:c.-21-801G= NP_998817.1:n.-21-801G=
NM_213653.3:c.331G= NP_998818.1:p.Glu111=
XM_005272932.1:c.331G= XP_005272989.1:p.Glu111=
NM_001316767.2:c.-22+197G= NP_001303696.1:n.-22+197G=
NM_145277.5:c.-9G= NP_660320.3:n.-9G=
NM_202004.4:c.-22+197G= NP_973733.1:n.-22+197G=
NM_213652.4:c.-21-801G= NP_998817.1:n.-21-801G=
NM_001379352.1:c.331G= NP_001366281.1:p.Glu111=
NM_213653.4:c.331G= MANE Select NP_998818.1:p.Glu111=