Canonical Allele Identifier: CA1335314082

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534253C= , CM000664.2:g.232534253C=	GRCh38
NC_000002.11:g.233398963C= , CM000664.1:g.233398963C=	GRCh37
NC_000002.10:g.233107207C=	NCBI36
NG_008028.1:g.13042C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1282C= MANE Select	ENSP00000258385.3:p.Gln428=
ENST00000258385.7:c.1282C=	ENSP00000258385.3:p.Gln428=
ENST00000441621.6:c.*464C=	ENSP00000408819.2:n.*464C=
ENST00000446616.1:c.*923C=	ENSP00000410801.1:n.*923C=
ENST00000543200.5:c.1237C=	ENSP00000438380.1:p.Gln413=
NM_000751.2:c.1282C=	NP_000742.1:p.Gln428=
NM_001256657.1:c.1237C=	NP_001243586.1:p.Gln413=
NM_001311195.1:c.700C=	NP_001298124.1:p.Gln234=
NM_001311196.1:c.979C=	NP_001298125.1:p.Gln327=
NR_046333.1:c.-4294966269C=
NR_046334.1:c.-4294965990C=
XM_011510524.1:c.901C=	XP_011508826.1:p.Gln301=
XM_011510524.2:c.901C=	XP_011508826.1:p.Gln301=
NM_000751.3:c.1282C= MANE Select	NP_000742.1:p.Gln428=
NM_001311195.2:c.700C=	NP_001298124.1:p.Gln234=
NM_001311196.2:c.979C=	NP_001298125.1:p.Gln327=
NM_001256657.2:c.1237C=	NP_001243586.1:p.Gln413=