Canonical Allele Identifier: CA1335313958
Gene: CHRND HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232533987A= , CM000664.2:g.232533987A= GRCh38
NC_000002.11:g.233398697A= , CM000664.1:g.233398697A= GRCh37
NC_000002.10:g.233106941A= NCBI36
NG_008028.1:g.12776A=

Transcript Alleles

HGVS Amino-acid change
ENST00000258385.8:c.1104A= MANE Select ENSP00000258385.3:p.Gly368=
ENST00000258385.7:c.1104A= ENSP00000258385.3:p.Gly368=
ENST00000441621.6:c.*286A= ENSP00000408819.2:n.*286A=
ENST00000446616.1:c.*745A= ENSP00000410801.1:n.*745A=
ENST00000543200.5:c.1059A= ENSP00000438380.1:p.Gly353=
NM_000751.2:c.1104A= NP_000742.1:p.Gly368=
NM_001256657.1:c.1059A= NP_001243586.1:p.Gly353=
NM_001311195.1:c.522A= NP_001298124.1:p.Gly174=
NM_001311196.1:c.801A= NP_001298125.1:p.Gly267=
NR_046333.1:c.-4294966447A=
NR_046334.1:c.-4294966168A=
XM_011510524.1:c.723A= XP_011508826.1:p.Gly241=
XM_011510524.2:c.723A= XP_011508826.1:p.Gly241=
NM_000751.3:c.1104A= MANE Select NP_000742.1:p.Gly368=
NM_001311195.2:c.522A= NP_001298124.1:p.Gly174=
NM_001311196.2:c.801A= NP_001298125.1:p.Gly267=
NM_001256657.2:c.1059A= NP_001243586.1:p.Gly353=