Canonical Allele Identifier: CA1335314007
Gene: CHRND HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232534099G= , CM000664.2:g.232534099G= GRCh38
NC_000002.11:g.233398809G= , CM000664.1:g.233398809G= GRCh37
NC_000002.10:g.233107053G= NCBI36
NG_008028.1:g.12888G=

Transcript Alleles

HGVS Amino-acid change
ENST00000258385.8:c.1216G= MANE Select ENSP00000258385.3:p.Glu406=
ENST00000258385.7:c.1216G= ENSP00000258385.3:p.Glu406=
ENST00000441621.6:c.*398G= ENSP00000408819.2:n.*398G=
ENST00000446616.1:c.*857G= ENSP00000410801.1:n.*857G=
ENST00000543200.5:c.1171G= ENSP00000438380.1:p.Glu391=
NM_000751.2:c.1216G= NP_000742.1:p.Glu406=
NM_001256657.1:c.1171G= NP_001243586.1:p.Glu391=
NM_001311195.1:c.634G= NP_001298124.1:p.Glu212=
NM_001311196.1:c.913G= NP_001298125.1:p.Glu305=
NR_046333.1:c.-4294966335G=
NR_046334.1:c.-4294966056G=
XM_011510524.1:c.835G= XP_011508826.1:p.Glu279=
XM_011510524.2:c.835G= XP_011508826.1:p.Glu279=
NM_000751.3:c.1216G= MANE Select NP_000742.1:p.Glu406=
NM_001311195.2:c.634G= NP_001298124.1:p.Glu212=
NM_001311196.2:c.913G= NP_001298125.1:p.Glu305=
NM_001256657.2:c.1171G= NP_001243586.1:p.Glu391=