Canonical Allele Identifier: CA1198821358
Gene: HJV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.146019411C= , CM000663.2:g.146019411C= GRCh38
NC_000001.10:g.145415602G= , CM000663.1:g.145415602G= GRCh37
NC_000001.9:g.144126959G= NCBI36
NG_011568.1:g.7412G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336751.11:c.421G= MANE Select ENSP00000337014.5:p.Gly141=
ENST00000636675.1:c.-22+287G= ENSP00000490072.1:n.-22+287G=
ENST00000336751.10:c.421G= ENSP00000337014.5:p.Gly141=
ENST00000357836.5:c.82G= ENSP00000350495.5:p.Gly28=
ENST00000475797.1:c.-21-711G= ENSP00000425716.1:n.-21-711G=
ENST00000497365.5:c.-22+287G= ENSP00000421820.1:n.-22+287G=
ENST00000634927.1:c.134+287G= ENSP00000489347.1:n.134+287G=
NM_001316767.1:c.-22+287G= NP_001303696.1:n.-22+287G=
NM_145277.4:c.82G= NP_660320.3:p.Gly28=
NM_202004.3:c.-22+287G= NP_973733.1:n.-22+287G=
NM_213652.3:c.-21-711G= NP_998817.1:n.-21-711G=
NM_213653.3:c.421G= NP_998818.1:p.Gly141=
XM_005272932.1:c.421G= XP_005272989.1:p.Gly141=
NM_001316767.2:c.-22+287G= NP_001303696.1:n.-22+287G=
NM_145277.5:c.82G= NP_660320.3:p.Gly28=
NM_202004.4:c.-22+287G= NP_973733.1:n.-22+287G=
NM_213652.4:c.-21-711G= NP_998817.1:n.-21-711G=
NM_001379352.1:c.421G= NP_001366281.1:p.Gly141=
NM_213653.4:c.421G= MANE Select NP_998818.1:p.Gly141=