Canonical Allele Identifier: CA2168280
Gene: CHRND HGNC NCBI

Linked Data

dbSNP Id: rs145920855

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232534045G>A , CM000664.2:g.232534045G>A GRCh38
NC_000002.11:g.233398755G>A , CM000664.1:g.233398755G>A GRCh37
NC_000002.10:g.233106999G>A NCBI36
NG_008028.1:g.12834G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258385.8:c.1162G>A MANE Select ENSP00000258385.3:p.Glu388Lys
ENST00000258385.7:c.1162G>A ENSP00000258385.3:p.Glu388Lys
ENST00000441621.6:c.*344G>A ENSP00000408819.2:n.*344G>A
ENST00000446616.1:c.*803G>A ENSP00000410801.1:n.*803G>A
ENST00000543200.5:c.1117G>A ENSP00000438380.1:p.Glu373Lys
NM_000751.2:c.1162G>A NP_000742.1:p.Glu388Lys
NM_001256657.1:c.1117G>A NP_001243586.1:p.Glu373Lys
NM_001311195.1:c.580G>A NP_001298124.1:p.Glu194Lys
NM_001311196.1:c.859G>A NP_001298125.1:p.Glu287Lys
NR_046333.1:c.-4294966389G>A
NR_046334.1:c.-4294966110G>A
XM_011510524.1:c.781G>A XP_011508826.1:p.Glu261Lys
XM_011510524.2:c.781G>A XP_011508826.1:p.Glu261Lys
NM_000751.3:c.1162G>A MANE Select NP_000742.1:p.Glu388Lys
NM_001311195.2:c.580G>A NP_001298124.1:p.Glu194Lys
NM_001311196.2:c.859G>A NP_001298125.1:p.Glu287Lys
NM_001256657.2:c.1117G>A NP_001243586.1:p.Glu373Lys