Canonical Allele Identifier: CA1335313986

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534047G= , CM000664.2:g.232534047G=	GRCh38
NC_000002.11:g.233398757G= , CM000664.1:g.233398757G=	GRCh37
NC_000002.10:g.233107001G=	NCBI36
NG_008028.1:g.12836G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1164G= MANE Select	ENSP00000258385.3:p.Glu388=
ENST00000258385.7:c.1164G=	ENSP00000258385.3:p.Glu388=
ENST00000441621.6:c.*346G=	ENSP00000408819.2:n.*346G=
ENST00000446616.1:c.*805G=	ENSP00000410801.1:n.*805G=
ENST00000543200.5:c.1119G=	ENSP00000438380.1:p.Glu373=
NM_000751.2:c.1164G=	NP_000742.1:p.Glu388=
NM_001256657.1:c.1119G=	NP_001243586.1:p.Glu373=
NM_001311195.1:c.582G=	NP_001298124.1:p.Glu194=
NM_001311196.1:c.861G=	NP_001298125.1:p.Glu287=
NR_046333.1:c.-4294966387G=
NR_046334.1:c.-4294966108G=
XM_011510524.1:c.783G=	XP_011508826.1:p.Glu261=
XM_011510524.2:c.783G=	XP_011508826.1:p.Glu261=
NM_000751.3:c.1164G= MANE Select	NP_000742.1:p.Glu388=
NM_001311195.2:c.582G=	NP_001298124.1:p.Glu194=
NM_001311196.2:c.861G=	NP_001298125.1:p.Glu287=
NM_001256657.2:c.1119G=	NP_001243586.1:p.Glu373=