Canonical Allele Identifier: CA1335313975
Gene: CHRND HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232534014G= , CM000664.2:g.232534014G= GRCh38
NC_000002.11:g.233398724G= , CM000664.1:g.233398724G= GRCh37
NC_000002.10:g.233106968G= NCBI36
NG_008028.1:g.12803G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258385.8:c.1131G= MANE Select ENSP00000258385.3:p.Arg377=
ENST00000258385.7:c.1131G= ENSP00000258385.3:p.Arg377=
ENST00000441621.6:c.*313G= ENSP00000408819.2:n.*313G=
ENST00000446616.1:c.*772G= ENSP00000410801.1:n.*772G=
ENST00000543200.5:c.1086G= ENSP00000438380.1:p.Arg362=
NM_000751.2:c.1131G= NP_000742.1:p.Arg377=
NM_001256657.1:c.1086G= NP_001243586.1:p.Arg362=
NM_001311195.1:c.549G= NP_001298124.1:p.Arg183=
NM_001311196.1:c.828G= NP_001298125.1:p.Arg276=
NR_046333.1:c.-4294966420G=
NR_046334.1:c.-4294966141G=
XM_011510524.1:c.750G= XP_011508826.1:p.Arg250=
XM_011510524.2:c.750G= XP_011508826.1:p.Arg250=
NM_000751.3:c.1131G= MANE Select NP_000742.1:p.Arg377=
NM_001311195.2:c.549G= NP_001298124.1:p.Arg183=
NM_001311196.2:c.828G= NP_001298125.1:p.Arg276=
NM_001256657.2:c.1086G= NP_001243586.1:p.Arg362=