Canonical Allele Identifier: CA1335313993

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534069C= , CM000664.2:g.232534069C=	GRCh38
NC_000002.11:g.233398779C= , CM000664.1:g.233398779C=	GRCh37
NC_000002.10:g.233107023C=	NCBI36
NG_008028.1:g.12858C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1186C= MANE Select	ENSP00000258385.3:p.Arg396=
ENST00000258385.7:c.1186C=	ENSP00000258385.3:p.Arg396=
ENST00000441621.6:c.*368C=	ENSP00000408819.2:n.*368C=
ENST00000446616.1:c.*827C=	ENSP00000410801.1:n.*827C=
ENST00000543200.5:c.1141C=	ENSP00000438380.1:p.Arg381=
NM_000751.2:c.1186C=	NP_000742.1:p.Arg396=
NM_001256657.1:c.1141C=	NP_001243586.1:p.Arg381=
NM_001311195.1:c.604C=	NP_001298124.1:p.Arg202=
NM_001311196.1:c.883C=	NP_001298125.1:p.Arg295=
NR_046333.1:c.-4294966365C=
NR_046334.1:c.-4294966086C=
XM_011510524.1:c.805C=	XP_011508826.1:p.Arg269=
XM_011510524.2:c.805C=	XP_011508826.1:p.Arg269=
NM_000751.3:c.1186C= MANE Select	NP_000742.1:p.Arg396=
NM_001311195.2:c.604C=	NP_001298124.1:p.Arg202=
NM_001311196.2:c.883C=	NP_001298125.1:p.Arg295=
NM_001256657.2:c.1141C=	NP_001243586.1:p.Arg381=