Canonical Allele Identifier: CA1335313961
Gene: CHRND HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232533989C= , CM000664.2:g.232533989C= GRCh38
NC_000002.11:g.233398699C= , CM000664.1:g.233398699C= GRCh37
NC_000002.10:g.233106943C= NCBI36
NG_008028.1:g.12778C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000258385.8:c.1106C= MANE Select ENSP00000258385.3:p.Pro369=
ENST00000258385.7:c.1106C= ENSP00000258385.3:p.Pro369=
ENST00000441621.6:c.*288C= ENSP00000408819.2:n.*288C=
ENST00000446616.1:c.*747C= ENSP00000410801.1:n.*747C=
ENST00000543200.5:c.1061C= ENSP00000438380.1:p.Pro354=
NM_000751.2:c.1106C= NP_000742.1:p.Pro369=
NM_001256657.1:c.1061C= NP_001243586.1:p.Pro354=
NM_001311195.1:c.524C= NP_001298124.1:p.Pro175=
NM_001311196.1:c.803C= NP_001298125.1:p.Pro268=
NR_046333.1:c.-4294966445C=
NR_046334.1:c.-4294966166C=
XM_011510524.1:c.725C= XP_011508826.1:p.Pro242=
XM_011510524.2:c.725C= XP_011508826.1:p.Pro242=
NM_000751.3:c.1106C= MANE Select NP_000742.1:p.Pro369=
NM_001311195.2:c.524C= NP_001298124.1:p.Pro175=
NM_001311196.2:c.803C= NP_001298125.1:p.Pro268=
NM_001256657.2:c.1061C= NP_001243586.1:p.Pro354=