Canonical Allele Identifier: CA1198821372
Gene: HJV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.146019432_146019433delinsCG , CM000663.2:g.146019432_146019433delinsCG GRCh38
NC_000001.10:g.145415580_145415581delinsCG , CM000663.1:g.145415580_145415581delinsCG GRCh37
NC_000001.9:g.144126937_144126938delinsCG NCBI36
NG_011568.1:g.7390_7391delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000336751.11:c.399_400delinsCG MANE Select ENSP00000337014.5:p.Pro133=
ENST00000636675.1:c.-22+265_-22+266delinsCG ENSP00000490072.1:n.-22+265_-22+266delinsCG
ENST00000336751.10:c.399_400delinsCG ENSP00000337014.5:p.Pro133=
ENST00000357836.5:c.60_61delinsCG ENSP00000350495.5:p.Pro20=
ENST00000475797.1:c.-21-733_-21-732delinsCG ENSP00000425716.1:n.-21-733_-21-732delinsCG
ENST00000497365.5:c.-22+265_-22+266delinsCG ENSP00000421820.1:n.-22+265_-22+266delinsCG
ENST00000634927.1:c.134+265_134+266delinsCG ENSP00000489347.1:n.134+265_134+266delinsCG
NM_001316767.1:c.-22+265_-22+266delinsCG NP_001303696.1:n.-22+265_-22+266delinsCG
NM_145277.4:c.60_61delinsCG NP_660320.3:p.Pro20=
NM_202004.3:c.-22+265_-22+266delinsCG NP_973733.1:n.-22+265_-22+266delinsCG
NM_213652.3:c.-21-733_-21-732delinsCG NP_998817.1:n.-21-733_-21-732delinsCG
NM_213653.3:c.399_400delinsCG NP_998818.1:p.Pro133=
XM_005272932.1:c.399_400delinsCG XP_005272989.1:p.Pro133=
NM_001316767.2:c.-22+265_-22+266delinsCG NP_001303696.1:n.-22+265_-22+266delinsCG
NM_145277.5:c.60_61delinsCG NP_660320.3:p.Pro20=
NM_202004.4:c.-22+265_-22+266delinsCG NP_973733.1:n.-22+265_-22+266delinsCG
NM_213652.4:c.-21-733_-21-732delinsCG NP_998817.1:n.-21-733_-21-732delinsCG
NM_001379352.1:c.399_400delinsCG NP_001366281.1:p.Pro133=
NM_213653.4:c.399_400delinsCG MANE Select NP_998818.1:p.Pro133=