Canonical Allele Identifier: CA1335314463
Gene: CHRND HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232535135A= , CM000664.2:g.232535135A= GRCh38
NC_000002.11:g.233399845A= , CM000664.1:g.233399845A= GRCh37
NC_000002.10:g.233108089A= NCBI36
NG_008028.1:g.13924A=
NG_012954.1:g.409A=
NG_012954.2:g.444A=

Transcript Alleles

HGVS Amino-acid change
ENST00000258385.8:c.1377A= MANE Select ENSP00000258385.3:p.Lys459=
ENST00000258385.7:c.1377A= ENSP00000258385.3:p.Lys459=
ENST00000441621.6:c.*559A= ENSP00000408819.2:n.*559A=
ENST00000446616.1:c.*1018A= ENSP00000410801.1:n.*1018A=
ENST00000543200.5:c.1332A= ENSP00000438380.1:p.Lys444=
NM_000751.2:c.1377A= NP_000742.1:p.Lys459=
NM_001256657.1:c.1332A= NP_001243586.1:p.Lys444=
NM_001311195.1:c.795A= NP_001298124.1:p.Lys265=
NM_001311196.1:c.1074A= NP_001298125.1:p.Lys358=
NR_046333.1:c.-4294966174A=
NR_046334.1:c.-4294965895A=
XM_011510524.1:c.996A= XP_011508826.1:p.Lys332=
XM_011510524.2:c.996A= XP_011508826.1:p.Lys332=
NM_000751.3:c.1377A= MANE Select NP_000742.1:p.Lys459=
NM_001311195.2:c.795A= NP_001298124.1:p.Lys265=
NM_001311196.2:c.1074A= NP_001298125.1:p.Lys358=
NM_001256657.2:c.1332A= NP_001243586.1:p.Lys444=