Canonical Allele Identifier: CA1335314465

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232535138C= , CM000664.2:g.232535138C=	GRCh38
NC_000002.11:g.233399848C= , CM000664.1:g.233399848C=	GRCh37
NC_000002.10:g.233108092C=	NCBI36
NG_008028.1:g.13927C=
NG_012954.1:g.412C=
NG_012954.2:g.447C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258385.8:c.1380C= MANE Select	ENSP00000258385.3:p.Asp460=
ENST00000258385.7:c.1380C=	ENSP00000258385.3:p.Asp460=
ENST00000441621.6:c.*562C=	ENSP00000408819.2:n.*562C=
ENST00000446616.1:c.*1021C=	ENSP00000410801.1:n.*1021C=
ENST00000543200.5:c.1335C=	ENSP00000438380.1:p.Asp445=
NM_000751.2:c.1380C=	NP_000742.1:p.Asp460=
NM_001256657.1:c.1335C=	NP_001243586.1:p.Asp445=
NM_001311195.1:c.798C=	NP_001298124.1:p.Asp266=
NM_001311196.1:c.1077C=	NP_001298125.1:p.Asp359=
NR_046333.1:c.-4294966171C=
NR_046334.1:c.-4294965892C=
XM_011510524.1:c.999C=	XP_011508826.1:p.Asp333=
XM_011510524.2:c.999C=	XP_011508826.1:p.Asp333=
NM_000751.3:c.1380C= MANE Select	NP_000742.1:p.Asp460=
NM_001311195.2:c.798C=	NP_001298124.1:p.Asp266=
NM_001311196.2:c.1077C=	NP_001298125.1:p.Asp359=
NM_001256657.2:c.1335C=	NP_001243586.1:p.Asp445=