Canonical Allele Identifier: CA1198821306
Gene: HJV HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.146019311_146019312delinsTG , CM000663.2:g.146019311_146019312delinsTG GRCh38
NC_000001.10:g.145415701_145415702delinsCA , CM000663.1:g.145415701_145415702delinsCA GRCh37
NC_000001.9:g.144127058_144127059delinsCA NCBI36
NG_011568.1:g.7511_7512delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000336751.11:c.520_521delinsCA MANE Select ENSP00000337014.5:p.His174=
ENST00000636675.1:c.-22+386_-22+387delinsCA ENSP00000490072.1:n.-22+386_-22+387delinsCA
ENST00000336751.10:c.520_521delinsCA ENSP00000337014.5:p.His174=
ENST00000357836.5:c.181_182delinsCA ENSP00000350495.5:p.His61=
ENST00000475797.1:c.-21-612_-21-611delinsCA ENSP00000425716.1:n.-21-612_-21-611delinsCA
ENST00000497365.5:c.-22+386_-22+387delinsCA ENSP00000421820.1:n.-22+386_-22+387delinsCA
ENST00000634927.1:c.134+386_134+387delinsCA ENSP00000489347.1:n.134+386_134+387delinsCA
NM_001316767.1:c.-22+386_-22+387delinsCA NP_001303696.1:n.-22+386_-22+387delinsCA
NM_145277.4:c.181_182delinsCA NP_660320.3:p.His61=
NM_202004.3:c.-22+386_-22+387delinsCA NP_973733.1:n.-22+386_-22+387delinsCA
NM_213652.3:c.-21-612_-21-611delinsCA NP_998817.1:n.-21-612_-21-611delinsCA
NM_213653.3:c.520_521delinsCA NP_998818.1:p.His174=
XM_005272932.1:c.520_521delinsCA XP_005272989.1:p.His174=
NM_001316767.2:c.-22+386_-22+387delinsCA NP_001303696.1:n.-22+386_-22+387delinsCA
NM_145277.5:c.181_182delinsCA NP_660320.3:p.His61=
NM_202004.4:c.-22+386_-22+387delinsCA NP_973733.1:n.-22+386_-22+387delinsCA
NM_213652.4:c.-21-612_-21-611delinsCA NP_998817.1:n.-21-612_-21-611delinsCA
NM_001379352.1:c.520_521delinsCA NP_001366281.1:p.His174=
NM_213653.4:c.520_521delinsCA MANE Select NP_998818.1:p.His174=