Canonical Allele Identifier: CA1198821351
Gene: HJV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.146019401G= , CM000663.2:g.146019401G= GRCh38
NC_000001.10:g.145415612C= , CM000663.1:g.145415612C= GRCh37
NC_000001.9:g.144126969C= NCBI36
NG_011568.1:g.7422C=

Transcript Alleles

HGVS Amino-acid change
ENST00000336751.11:c.431C= MANE Select ENSP00000337014.5:p.Ala144=
ENST00000636675.1:c.-22+297C= ENSP00000490072.1:n.-22+297C=
ENST00000336751.10:c.431C= ENSP00000337014.5:p.Ala144=
ENST00000357836.5:c.92C= ENSP00000350495.5:p.Ala31=
ENST00000475797.1:c.-21-701C= ENSP00000425716.1:n.-21-701C=
ENST00000497365.5:c.-22+297C= ENSP00000421820.1:n.-22+297C=
ENST00000634927.1:c.134+297C= ENSP00000489347.1:n.134+297C=
NM_001316767.1:c.-22+297C= NP_001303696.1:n.-22+297C=
NM_145277.4:c.92C= NP_660320.3:p.Ala31=
NM_202004.3:c.-22+297C= NP_973733.1:n.-22+297C=
NM_213652.3:c.-21-701C= NP_998817.1:n.-21-701C=
NM_213653.3:c.431C= NP_998818.1:p.Ala144=
XM_005272932.1:c.431C= XP_005272989.1:p.Ala144=
NM_001316767.2:c.-22+297C= NP_001303696.1:n.-22+297C=
NM_145277.5:c.92C= NP_660320.3:p.Ala31=
NM_202004.4:c.-22+297C= NP_973733.1:n.-22+297C=
NM_213652.4:c.-21-701C= NP_998817.1:n.-21-701C=
NM_001379352.1:c.431C= NP_001366281.1:p.Ala144=
NM_213653.4:c.431C= MANE Select NP_998818.1:p.Ala144=