Canonical Allele Identifier: CA2168295
Gene: CHRND HGNC NCBI

Linked Data

dbSNP Id: rs752209967

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232534108G>A , CM000664.2:g.232534108G>A GRCh38
NC_000002.11:g.233398818G>A , CM000664.1:g.233398818G>A GRCh37
NC_000002.10:g.233107062G>A NCBI36
NG_008028.1:g.12897G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000258385.8:c.1225G>A MANE Select ENSP00000258385.3:p.Gly409Arg
ENST00000258385.7:c.1225G>A ENSP00000258385.3:p.Gly409Arg
ENST00000441621.6:c.*407G>A ENSP00000408819.2:n.*407G>A
ENST00000446616.1:c.*866G>A ENSP00000410801.1:n.*866G>A
ENST00000543200.5:c.1180G>A ENSP00000438380.1:p.Gly394Arg
NM_000751.2:c.1225G>A NP_000742.1:p.Gly409Arg
NM_001256657.1:c.1180G>A NP_001243586.1:p.Gly394Arg
NM_001311195.1:c.643G>A NP_001298124.1:p.Gly215Arg
NM_001311196.1:c.922G>A NP_001298125.1:p.Gly308Arg
NR_046333.1:c.-4294966326G>A
NR_046334.1:c.-4294966047G>A
XM_011510524.1:c.844G>A XP_011508826.1:p.Gly282Arg
XM_011510524.2:c.844G>A XP_011508826.1:p.Gly282Arg
NM_000751.3:c.1225G>A MANE Select NP_000742.1:p.Gly409Arg
NM_001311195.2:c.643G>A NP_001298124.1:p.Gly215Arg
NM_001311196.2:c.922G>A NP_001298125.1:p.Gly308Arg
NM_001256657.2:c.1180G>A NP_001243586.1:p.Gly394Arg