Canonical Allele Identifier: CA1335310410

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232528271_232528273delinsGAC , CM000664.2:g.232528271_232528273delinsGAC	GRCh38
NC_000002.11:g.233392981_233392983delinsGAC , CM000664.1:g.233392981_233392983delinsGAC	GRCh37
NC_000002.10:g.233101225_233101227delinsGAC	NCBI36
NG_008028.1:g.7060_7062delinsGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.253_255delinsGAC MANE Select	ENSP00000258385.3:p.Asp85=
ENST00000258385.7:c.253_255delinsGAC	ENSP00000258385.3:p.Asp85=
ENST00000412233.5:c.253_255delinsGAC	ENSP00000398143.1:p.Asp85=
ENST00000441621.6:c.253_255delinsGAC	ENSP00000408819.2:p.Asp85=
ENST00000446616.1:c.253_255delinsGAC	ENSP00000410801.1:p.Asp85=
ENST00000449596.5:c.208_210delinsGAC	ENSP00000404950.1:p.Asp70=
ENST00000543200.5:c.208_210delinsGAC	ENSP00000438380.1:p.Asp70=
NM_000751.2:c.253_255delinsGAC	NP_000742.1:p.Asp85=
NM_001256657.1:c.208_210delinsGAC	NP_001243586.1:p.Asp70=
NM_001311195.1:c.-19_-17delinsGAC	NP_001298124.1:n.-19_-17delinsGAC
NM_001311196.1:c.-19_-17delinsGAC	NP_001298125.1:n.-19_-17delinsGAC
NR_046333.1:c.-4294966987_-4294966985delinsGAC
NR_046334.1:c.-4294966987_-4294966985delinsGAC
XM_011510524.1:c.-19_-17delinsGAC	XP_011508826.1:n.-19_-17delinsGAC
XM_011510524.2:c.-19_-17delinsGAC	XP_011508826.1:n.-19_-17delinsGAC
NM_000751.3:c.253_255delinsGAC MANE Select	NP_000742.1:p.Asp85=
NM_001311195.2:c.-19_-17delinsGAC	NP_001298124.1:n.-19_-17delinsGAC
NM_001311196.2:c.-19_-17delinsGAC	NP_001298125.1:n.-19_-17delinsGAC
NM_001256657.2:c.208_210delinsGAC	NP_001243586.1:p.Asp70=