Canonical Allele Identifier: CA1335314464

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232535136G= , CM000664.2:g.232535136G=	GRCh38
NC_000002.11:g.233399846G= , CM000664.1:g.233399846G=	GRCh37
NC_000002.10:g.233108090G=	NCBI36
NG_008028.1:g.13925G=
NG_012954.1:g.410G=
NG_012954.2:g.445G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258385.8:c.1378G= MANE Select	ENSP00000258385.3:p.Asp460=
ENST00000258385.7:c.1378G=	ENSP00000258385.3:p.Asp460=
ENST00000441621.6:c.*560G=	ENSP00000408819.2:n.*560G=
ENST00000446616.1:c.*1019G=	ENSP00000410801.1:n.*1019G=
ENST00000543200.5:c.1333G=	ENSP00000438380.1:p.Asp445=
NM_000751.2:c.1378G=	NP_000742.1:p.Asp460=
NM_001256657.1:c.1333G=	NP_001243586.1:p.Asp445=
NM_001311195.1:c.796G=	NP_001298124.1:p.Asp266=
NM_001311196.1:c.1075G=	NP_001298125.1:p.Asp359=
NR_046333.1:c.-4294966173G=
NR_046334.1:c.-4294965894G=
XM_011510524.1:c.997G=	XP_011508826.1:p.Asp333=
XM_011510524.2:c.997G=	XP_011508826.1:p.Asp333=
NM_000751.3:c.1378G= MANE Select	NP_000742.1:p.Asp460=
NM_001311195.2:c.796G=	NP_001298124.1:p.Asp266=
NM_001311196.2:c.1075G=	NP_001298125.1:p.Asp359=
NM_001256657.2:c.1333G=	NP_001243586.1:p.Asp445=