Canonical Allele Identifier: CA1335314017

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534118G= , CM000664.2:g.232534118G=	GRCh38
NC_000002.11:g.233398828G= , CM000664.1:g.233398828G=	GRCh37
NC_000002.10:g.233107072G=	NCBI36
NG_008028.1:g.12907G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1235G= MANE Select	ENSP00000258385.3:p.Arg412=
ENST00000258385.7:c.1235G=	ENSP00000258385.3:p.Arg412=
ENST00000441621.6:c.*417G=	ENSP00000408819.2:n.*417G=
ENST00000446616.1:c.*876G=	ENSP00000410801.1:n.*876G=
ENST00000543200.5:c.1190G=	ENSP00000438380.1:p.Arg397=
NM_000751.2:c.1235G=	NP_000742.1:p.Arg412=
NM_001256657.1:c.1190G=	NP_001243586.1:p.Arg397=
NM_001311195.1:c.653G=	NP_001298124.1:p.Arg218=
NM_001311196.1:c.932G=	NP_001298125.1:p.Arg311=
NR_046333.1:c.-4294966316G=
NR_046334.1:c.-4294966037G=
XM_011510524.1:c.854G=	XP_011508826.1:p.Arg285=
XM_011510524.2:c.854G=	XP_011508826.1:p.Arg285=
NM_000751.3:c.1235G= MANE Select	NP_000742.1:p.Arg412=
NM_001311195.2:c.653G=	NP_001298124.1:p.Arg218=
NM_001311196.2:c.932G=	NP_001298125.1:p.Arg311=
NM_001256657.2:c.1190G=	NP_001243586.1:p.Arg397=