Canonical Allele Identifier: CA342135500
Gene: HJV HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.146018434G>C , CM000663.2:g.146018434G>C GRCh38
NC_000001.10:g.145416579C>G , CM000663.1:g.145416579C>G GRCh37
NC_000001.9:g.144127936C>G NCBI36
NG_011568.1:g.8389C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000336751.11:c.924C>G MANE Select ENSP00000337014.5:p.Phe308Leu
ENST00000636675.1:c.246C>G ENSP00000490072.1:p.Phe82Leu
ENST00000336751.10:c.924C>G ENSP00000337014.5:p.Phe308Leu
ENST00000357836.5:c.585C>G ENSP00000350495.5:p.Phe195Leu
ENST00000475797.1:c.246C>G ENSP00000425716.1:p.Phe82Leu
ENST00000497365.5:c.246C>G ENSP00000421820.1:p.Phe82Leu
NM_001316767.1:c.246C>G NP_001303696.1:p.Phe82Leu
NM_145277.4:c.585C>G NP_660320.3:p.Phe195Leu
NM_202004.3:c.246C>G NP_973733.1:p.Phe82Leu
NM_213652.3:c.246C>G NP_998817.1:p.Phe82Leu
NM_213653.3:c.924C>G NP_998818.1:p.Phe308Leu
XM_005272932.1:c.924C>G XP_005272989.1:p.Phe308Leu
NM_001316767.2:c.246C>G NP_001303696.1:p.Phe82Leu
NM_145277.5:c.585C>G NP_660320.3:p.Phe195Leu
NM_202004.4:c.246C>G NP_973733.1:p.Phe82Leu
NM_213652.4:c.246C>G NP_998817.1:p.Phe82Leu
NM_001379352.1:c.924C>G NP_001366281.1:p.Phe308Leu
NM_213653.4:c.924C>G MANE Select NP_998818.1:p.Phe308Leu