Canonical Allele Identifier: CA350997378
Gene: CHRND HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232528263G>C , CM000664.2:g.232528263G>C GRCh38
NC_000002.11:g.233392973G>C , CM000664.1:g.233392973G>C GRCh37
NC_000002.10:g.233101217G>C NCBI36
NG_008028.1:g.7052G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258385.8:c.245G>C MANE Select ENSP00000258385.3:p.Gly82Ala
ENST00000258385.7:c.245G>C ENSP00000258385.3:p.Gly82Ala
ENST00000412233.5:c.245G>C ENSP00000398143.1:p.Gly82Ala
ENST00000441621.6:c.245G>C ENSP00000408819.2:p.Gly82Ala
ENST00000446616.1:c.245G>C ENSP00000410801.1:p.Gly82Ala
ENST00000449596.5:c.200G>C ENSP00000404950.1:p.Gly67Ala
ENST00000543200.5:c.200G>C ENSP00000438380.1:p.Gly67Ala
NM_000751.2:c.245G>C NP_000742.1:p.Gly82Ala
NM_001256657.1:c.200G>C NP_001243586.1:p.Gly67Ala
NM_001311195.1:c.-27G>C NP_001298124.1:n.-27G>C
NM_001311196.1:c.-27G>C NP_001298125.1:n.-27G>C
NR_046333.1:c.-4294966995G>C
NR_046334.1:c.-4294966995G>C
XM_011510524.1:c.-27G>C XP_011508826.1:n.-27G>C
XM_011510524.2:c.-27G>C XP_011508826.1:n.-27G>C
NM_000751.3:c.245G>C MANE Select NP_000742.1:p.Gly82Ala
NM_001311195.2:c.-27G>C NP_001298124.1:n.-27G>C
NM_001311196.2:c.-27G>C NP_001298125.1:n.-27G>C
NM_001256657.2:c.200G>C NP_001243586.1:p.Gly67Ala