Canonical Allele Identifier: CA2663623405

Gene: CHRND

Linked Data

• gnomAD v4: 2-232534102-C-CGG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534103_232534104dup , CM000664.2:g.232534103_232534104dup	GRCh38
NC_000002.11:g.233398813_233398814dup , CM000664.1:g.233398813_233398814dup	GRCh37
NC_000002.10:g.233107057_233107058dup	NCBI36
NG_008028.1:g.12892_12893dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1220_1221dup MANE Select	ENSP00000258385.3:p.His408GlyfsTer29
ENST00000258385.7:c.1220_1221dup	ENSP00000258385.3:p.His408GlyfsTer29
ENST00000441621.6:c.*402_*403dup	ENSP00000408819.2:n.*402_*403dup
ENST00000446616.1:c.*861_*862dup	ENSP00000410801.1:n.*861_*862dup
ENST00000543200.5:c.1175_1176dup	ENSP00000438380.1:p.His393GlyfsTer29
NM_000751.2:c.1220_1221dup	NP_000742.1:p.His408GlyfsTer29
NM_001256657.1:c.1175_1176dup	NP_001243586.1:p.His393GlyfsTer29
NM_001311195.1:c.638_639dup	NP_001298124.1:p.His214GlyfsTer29
NM_001311196.1:c.917_918dup	NP_001298125.1:p.His307GlyfsTer29
NR_046333.1:c.-4294966331_-4294966330dup
NR_046334.1:c.-4294966052_-4294966051dup
XM_011510524.1:c.839_840dup	XP_011508826.1:p.His281GlyfsTer29
XM_011510524.2:c.839_840dup	XP_011508826.1:p.His281GlyfsTer29
NM_000751.3:c.1220_1221dup MANE Select	NP_000742.1:p.His408GlyfsTer29
NM_001311195.2:c.638_639dup	NP_001298124.1:p.His214GlyfsTer29
NM_001311196.2:c.917_918dup	NP_001298125.1:p.His307GlyfsTer29
NM_001256657.2:c.1175_1176dup	NP_001243586.1:p.His393GlyfsTer29