Canonical Allele Identifier: CA2647575804
Gene: HJV HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.146019147_146019148insA , CM000663.2:g.146019147_146019148insA GRCh38
NC_000001.10:g.145415865_145415866insT , CM000663.1:g.145415865_145415866insT GRCh37
NC_000001.9:g.144127222_144127223insT NCBI36
NG_011568.1:g.7675_7676insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000336751.11:c.657+27_657+28insT MANE Select ENSP00000337014.5:n.657+27_657+28insT
ENST00000636675.1:c.-21-448_-21-447insT ENSP00000490072.1:n.-21-448_-21-447insT
ENST00000336751.10:c.657+27_657+28insT ENSP00000337014.5:n.657+27_657+28insT
ENST00000357836.5:c.318+27_318+28insT ENSP00000350495.5:n.318+27_318+28insT
ENST00000475797.1:c.-21-448_-21-447insT ENSP00000425716.1:n.-21-448_-21-447insT
ENST00000497365.5:c.-21-448_-21-447insT ENSP00000421820.1:n.-21-448_-21-447insT
ENST00000634927.1:c.135-448_135-447insT ENSP00000489347.1:n.135-448_135-447insT
NM_001316767.1:c.-21-448_-21-447insT NP_001303696.1:n.-21-448_-21-447insT
NM_145277.4:c.318+27_318+28insT NP_660320.3:n.318+27_318+28insT
NM_202004.3:c.-21-448_-21-447insT NP_973733.1:n.-21-448_-21-447insT
NM_213652.3:c.-21-448_-21-447insT NP_998817.1:n.-21-448_-21-447insT
NM_213653.3:c.657+27_657+28insT NP_998818.1:n.657+27_657+28insT
XM_005272932.1:c.657+27_657+28insT XP_005272989.1:n.657+27_657+28insT
NM_001316767.2:c.-21-448_-21-447insT NP_001303696.1:n.-21-448_-21-447insT
NM_145277.5:c.318+27_318+28insT NP_660320.3:n.318+27_318+28insT
NM_202004.4:c.-21-448_-21-447insT NP_973733.1:n.-21-448_-21-447insT
NM_213652.4:c.-21-448_-21-447insT NP_998817.1:n.-21-448_-21-447insT
NM_001379352.1:c.657+27_657+28insT NP_001366281.1:n.657+27_657+28insT
NM_213653.4:c.657+27_657+28insT MANE Select NP_998818.1:n.657+27_657+28insT