Canonical Allele Identifier: CA1335313960
Gene: CHRND HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232533988C= , CM000664.2:g.232533988C= GRCh38
NC_000002.11:g.233398698C= , CM000664.1:g.233398698C= GRCh37
NC_000002.10:g.233106942C= NCBI36
NG_008028.1:g.12777C=

Transcript Alleles

HGVS Amino-acid change
ENST00000258385.8:c.1105C= MANE Select ENSP00000258385.3:p.Pro369=
ENST00000258385.7:c.1105C= ENSP00000258385.3:p.Pro369=
ENST00000441621.6:c.*287C= ENSP00000408819.2:n.*287C=
ENST00000446616.1:c.*746C= ENSP00000410801.1:n.*746C=
ENST00000543200.5:c.1060C= ENSP00000438380.1:p.Pro354=
NM_000751.2:c.1105C= NP_000742.1:p.Pro369=
NM_001256657.1:c.1060C= NP_001243586.1:p.Pro354=
NM_001311195.1:c.523C= NP_001298124.1:p.Pro175=
NM_001311196.1:c.802C= NP_001298125.1:p.Pro268=
NR_046333.1:c.-4294966446C=
NR_046334.1:c.-4294966167C=
XM_011510524.1:c.724C= XP_011508826.1:p.Pro242=
XM_011510524.2:c.724C= XP_011508826.1:p.Pro242=
NM_000751.3:c.1105C= MANE Select NP_000742.1:p.Pro369=
NM_001311195.2:c.523C= NP_001298124.1:p.Pro175=
NM_001311196.2:c.802C= NP_001298125.1:p.Pro268=
NM_001256657.2:c.1060C= NP_001243586.1:p.Pro354=