Canonical Allele Identifier: CA1335314010

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534104G= , CM000664.2:g.232534104G=	GRCh38
NC_000002.11:g.233398814G= , CM000664.1:g.233398814G=	GRCh37
NC_000002.10:g.233107058G=	NCBI36
NG_008028.1:g.12893G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1221G= MANE Select	ENSP00000258385.3:p.Arg407=
ENST00000258385.7:c.1221G=	ENSP00000258385.3:p.Arg407=
ENST00000441621.6:c.*403G=	ENSP00000408819.2:n.*403G=
ENST00000446616.1:c.*862G=	ENSP00000410801.1:n.*862G=
ENST00000543200.5:c.1176G=	ENSP00000438380.1:p.Arg392=
NM_000751.2:c.1221G=	NP_000742.1:p.Arg407=
NM_001256657.1:c.1176G=	NP_001243586.1:p.Arg392=
NM_001311195.1:c.639G=	NP_001298124.1:p.Arg213=
NM_001311196.1:c.918G=	NP_001298125.1:p.Arg306=
NR_046333.1:c.-4294966330G=
NR_046334.1:c.-4294966051G=
XM_011510524.1:c.840G=	XP_011508826.1:p.Arg280=
XM_011510524.2:c.840G=	XP_011508826.1:p.Arg280=
NM_000751.3:c.1221G= MANE Select	NP_000742.1:p.Arg407=
NM_001311195.2:c.639G=	NP_001298124.1:p.Arg213=
NM_001311196.2:c.918G=	NP_001298125.1:p.Arg306=
NM_001256657.2:c.1176G=	NP_001243586.1:p.Arg392=