Canonical Allele Identifier: CA350997649
Gene: CHRND HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232528501C>G , CM000664.2:g.232528501C>G GRCh38
NC_000002.11:g.233393211C>G , CM000664.1:g.233393211C>G GRCh37
NC_000002.10:g.233101455C>G NCBI36
NG_008028.1:g.7290C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258385.8:c.354C>G MANE Select ENSP00000258385.3:p.Asn118Lys
ENST00000258385.7:c.354C>G ENSP00000258385.3:p.Asn118Lys
ENST00000412233.5:c.354C>G ENSP00000398143.1:p.Asn118Lys
ENST00000441621.6:c.354C>G ENSP00000408819.2:p.Asn118Lys
ENST00000446616.1:c.322C>G ENSP00000410801.1:p.Gln108Glu
ENST00000449596.5:c.309C>G ENSP00000404950.1:p.Asn103Lys
ENST00000543200.5:c.309C>G ENSP00000438380.1:p.Asn103Lys
NM_000751.2:c.354C>G NP_000742.1:p.Asn118Lys
NM_001256657.1:c.309C>G NP_001243586.1:p.Asn103Lys
NM_001311195.1:c.83C>G NP_001298124.1:p.Thr28Arg
NM_001311196.1:c.51C>G NP_001298125.1:p.Cys17Trp
NR_046333.1:c.-4294966886C>G
NR_046334.1:c.-4294966918C>G
XM_011510524.1:c.83C>G XP_011508826.1:p.Thr28Arg
XM_011510524.2:c.83C>G XP_011508826.1:p.Thr28Arg
NM_000751.3:c.354C>G MANE Select NP_000742.1:p.Asn118Lys
NM_001311195.2:c.83C>G NP_001298124.1:p.Thr28Arg
NM_001311196.2:c.51C>G NP_001298125.1:p.Cys17Trp
NM_001256657.2:c.309C>G NP_001243586.1:p.Asn103Lys