Canonical Allele Identifier: CA1335314087

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534269A= , CM000664.2:g.232534269A=	GRCh38
NC_000002.11:g.233398979A= , CM000664.1:g.233398979A=	GRCh37
NC_000002.10:g.233107223A=	NCBI36
NG_008028.1:g.13058A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1298A= MANE Select	ENSP00000258385.3:p.Asn433=
ENST00000258385.7:c.1298A=	ENSP00000258385.3:p.Asn433=
ENST00000441621.6:c.*480A=	ENSP00000408819.2:n.*480A=
ENST00000446616.1:c.*939A=	ENSP00000410801.1:n.*939A=
ENST00000543200.5:c.1253A=	ENSP00000438380.1:p.Asn418=
NM_000751.2:c.1298A=	NP_000742.1:p.Asn433=
NM_001256657.1:c.1253A=	NP_001243586.1:p.Asn418=
NM_001311195.1:c.716A=	NP_001298124.1:p.Asn239=
NM_001311196.1:c.995A=	NP_001298125.1:p.Asn332=
NR_046333.1:c.-4294966253A=
NR_046334.1:c.-4294965974A=
XM_011510524.1:c.917A=	XP_011508826.1:p.Asn306=
XM_011510524.2:c.917A=	XP_011508826.1:p.Asn306=
NM_000751.3:c.1298A= MANE Select	NP_000742.1:p.Asn433=
NM_001311195.2:c.716A=	NP_001298124.1:p.Asn239=
NM_001311196.2:c.995A=	NP_001298125.1:p.Asn332=
NM_001256657.2:c.1253A=	NP_001243586.1:p.Asn418=