Canonical Allele Identifier: CA1335314003
Gene: CHRND HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232534087G= , CM000664.2:g.232534087G= GRCh38
NC_000002.11:g.233398797G= , CM000664.1:g.233398797G= GRCh37
NC_000002.10:g.233107041G= NCBI36
NG_008028.1:g.12876G=

Transcript Alleles

HGVS Amino-acid change
ENST00000258385.8:c.1204G= MANE Select ENSP00000258385.3:p.Glu402=
ENST00000258385.7:c.1204G= ENSP00000258385.3:p.Glu402=
ENST00000441621.6:c.*386G= ENSP00000408819.2:n.*386G=
ENST00000446616.1:c.*845G= ENSP00000410801.1:n.*845G=
ENST00000543200.5:c.1159G= ENSP00000438380.1:p.Glu387=
NM_000751.2:c.1204G= NP_000742.1:p.Glu402=
NM_001256657.1:c.1159G= NP_001243586.1:p.Glu387=
NM_001311195.1:c.622G= NP_001298124.1:p.Glu208=
NM_001311196.1:c.901G= NP_001298125.1:p.Glu301=
NR_046333.1:c.-4294966347G=
NR_046334.1:c.-4294966068G=
XM_011510524.1:c.823G= XP_011508826.1:p.Glu275=
XM_011510524.2:c.823G= XP_011508826.1:p.Glu275=
NM_000751.3:c.1204G= MANE Select NP_000742.1:p.Glu402=
NM_001311195.2:c.622G= NP_001298124.1:p.Glu208=
NM_001311196.2:c.901G= NP_001298125.1:p.Glu301=
NM_001256657.2:c.1159G= NP_001243586.1:p.Glu387=