Canonical Allele Identifier: CA1335314106

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534330C= , CM000664.2:g.232534330C=	GRCh38
NC_000002.11:g.233399040C= , CM000664.1:g.233399040C=	GRCh37
NC_000002.10:g.233107284C=	NCBI36
NG_008028.1:g.13119C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1359C= MANE Select	ENSP00000258385.3:p.Asn453=
ENST00000258385.7:c.1359C=	ENSP00000258385.3:p.Asn453=
ENST00000441621.6:c.*541C=	ENSP00000408819.2:n.*541C=
ENST00000446616.1:c.*1000C=	ENSP00000410801.1:n.*1000C=
ENST00000543200.5:c.1314C=	ENSP00000438380.1:p.Asn438=
NM_000751.2:c.1359C=	NP_000742.1:p.Asn453=
NM_001256657.1:c.1314C=	NP_001243586.1:p.Asn438=
NM_001311195.1:c.777C=	NP_001298124.1:p.Asn259=
NM_001311196.1:c.1056C=	NP_001298125.1:p.Asn352=
NR_046333.1:c.-4294966192C=
NR_046334.1:c.-4294965913C=
XM_011510524.1:c.978C=	XP_011508826.1:p.Asn326=
XM_011510524.2:c.978C=	XP_011508826.1:p.Asn326=
NM_000751.3:c.1359C= MANE Select	NP_000742.1:p.Asn453=
NM_001311195.2:c.777C=	NP_001298124.1:p.Asn259=
NM_001311196.2:c.1056C=	NP_001298125.1:p.Asn352=
NM_001256657.2:c.1314C=	NP_001243586.1:p.Asn438=