Canonical Allele Identifier: CA1335314109

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534338A= , CM000664.2:g.232534338A=	GRCh38
NC_000002.11:g.233399048A= , CM000664.1:g.233399048A=	GRCh37
NC_000002.10:g.233107292A=	NCBI36
NG_008028.1:g.13127A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1367A= MANE Select	ENSP00000258385.3:p.Asn456=
ENST00000258385.7:c.1367A=	ENSP00000258385.3:p.Asn456=
ENST00000441621.6:c.*549A=	ENSP00000408819.2:n.*549A=
ENST00000446616.1:c.*1008A=	ENSP00000410801.1:n.*1008A=
ENST00000543200.5:c.1322A=	ENSP00000438380.1:p.Asn441=
NM_000751.2:c.1367A=	NP_000742.1:p.Asn456=
NM_001256657.1:c.1322A=	NP_001243586.1:p.Asn441=
NM_001311195.1:c.785A=	NP_001298124.1:p.Asn262=
NM_001311196.1:c.1064A=	NP_001298125.1:p.Asn355=
NR_046333.1:c.-4294966184A=
NR_046334.1:c.-4294965905A=
XM_011510524.1:c.986A=	XP_011508826.1:p.Asn329=
XM_011510524.2:c.986A=	XP_011508826.1:p.Asn329=
NM_000751.3:c.1367A= MANE Select	NP_000742.1:p.Asn456=
NM_001311195.2:c.785A=	NP_001298124.1:p.Asn262=
NM_001311196.2:c.1064A=	NP_001298125.1:p.Asn355=
NM_001256657.2:c.1322A=	NP_001243586.1:p.Asn441=