Canonical Allele Identifier: CA351005806
Gene: CHRND HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232534318G>C , CM000664.2:g.232534318G>C GRCh38
NC_000002.11:g.233399028G>C , CM000664.1:g.233399028G>C GRCh37
NC_000002.10:g.233107272G>C NCBI36
NG_008028.1:g.13107G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258385.8:c.1347G>C MANE Select ENSP00000258385.3:p.Met449Ile
ENST00000258385.7:c.1347G>C ENSP00000258385.3:p.Met449Ile
ENST00000441621.6:c.*529G>C ENSP00000408819.2:n.*529G>C
ENST00000446616.1:c.*988G>C ENSP00000410801.1:n.*988G>C
ENST00000543200.5:c.1302G>C ENSP00000438380.1:p.Met434Ile
NM_000751.2:c.1347G>C NP_000742.1:p.Met449Ile
NM_001256657.1:c.1302G>C NP_001243586.1:p.Met434Ile
NM_001311195.1:c.765G>C NP_001298124.1:p.Met255Ile
NM_001311196.1:c.1044G>C NP_001298125.1:p.Met348Ile
NR_046333.1:c.-4294966204G>C
NR_046334.1:c.-4294965925G>C
XM_011510524.1:c.966G>C XP_011508826.1:p.Met322Ile
XM_011510524.2:c.966G>C XP_011508826.1:p.Met322Ile
NM_000751.3:c.1347G>C MANE Select NP_000742.1:p.Met449Ile
NM_001311195.2:c.765G>C NP_001298124.1:p.Met255Ile
NM_001311196.2:c.1044G>C NP_001298125.1:p.Met348Ile
NM_001256657.2:c.1302G>C NP_001243586.1:p.Met434Ile