Canonical Allele Identifier: CA2663623607

Gene: CHRND

Linked Data

• gnomAD v4: 2-232534225-CCGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534227_232534229del , CM000664.2:g.232534227_232534229del	GRCh38
NC_000002.11:g.233398937_233398939del , CM000664.1:g.233398937_233398939del	GRCh37
NC_000002.10:g.233107181_233107183del	NCBI36
NG_008028.1:g.13016_13018del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1256_1258del MANE Select	ENSP00000258385.3:p.Arg419del
ENST00000258385.7:c.1256_1258del	ENSP00000258385.3:p.Arg419del
ENST00000441621.6:c.*438_*440del	ENSP00000408819.2:n.*438_*440del
ENST00000446616.1:c.*897_*899del	ENSP00000410801.1:n.*897_*899del
ENST00000543200.5:c.1211_1213del	ENSP00000438380.1:p.Arg404del
NM_000751.2:c.1256_1258del	NP_000742.1:p.Arg419del
NM_001256657.1:c.1211_1213del	NP_001243586.1:p.Arg404del
NM_001311195.1:c.674_676del	NP_001298124.1:p.Arg225del
NM_001311196.1:c.953_955del	NP_001298125.1:p.Arg318del
NR_046333.1:c.-4294966295_-4294966293del
NR_046334.1:c.-4294966016_-4294966014del
XM_011510524.1:c.875_877del	XP_011508826.1:p.Arg292del
XM_011510524.2:c.875_877del	XP_011508826.1:p.Arg292del
NM_000751.3:c.1256_1258del MANE Select	NP_000742.1:p.Arg419del
NM_001311195.2:c.674_676del	NP_001298124.1:p.Arg225del
NM_001311196.2:c.953_955del	NP_001298125.1:p.Arg318del
NM_001256657.2:c.1211_1213del	NP_001243586.1:p.Arg404del