Canonical Allele Identifier: CA1335314005
Gene: CHRND HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232534094A= , CM000664.2:g.232534094A= GRCh38
NC_000002.11:g.233398804A= , CM000664.1:g.233398804A= GRCh37
NC_000002.10:g.233107048A= NCBI36
NG_008028.1:g.12883A=

Transcript Alleles

HGVS Amino-acid change
ENST00000258385.8:c.1211A= MANE Select ENSP00000258385.3:p.Gln404=
ENST00000258385.7:c.1211A= ENSP00000258385.3:p.Gln404=
ENST00000441621.6:c.*393A= ENSP00000408819.2:n.*393A=
ENST00000446616.1:c.*852A= ENSP00000410801.1:n.*852A=
ENST00000543200.5:c.1166A= ENSP00000438380.1:p.Gln389=
NM_000751.2:c.1211A= NP_000742.1:p.Gln404=
NM_001256657.1:c.1166A= NP_001243586.1:p.Gln389=
NM_001311195.1:c.629A= NP_001298124.1:p.Gln210=
NM_001311196.1:c.908A= NP_001298125.1:p.Gln303=
NR_046333.1:c.-4294966340A=
NR_046334.1:c.-4294966061A=
XM_011510524.1:c.830A= XP_011508826.1:p.Gln277=
XM_011510524.2:c.830A= XP_011508826.1:p.Gln277=
NM_000751.3:c.1211A= MANE Select NP_000742.1:p.Gln404=
NM_001311195.2:c.629A= NP_001298124.1:p.Gln210=
NM_001311196.2:c.908A= NP_001298125.1:p.Gln303=
NM_001256657.2:c.1166A= NP_001243586.1:p.Gln389=