Canonical Allele Identifier: CA1335314462

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232535133A= , CM000664.2:g.232535133A=	GRCh38
NC_000002.11:g.233399843A= , CM000664.1:g.233399843A=	GRCh37
NC_000002.10:g.233108087A=	NCBI36
NG_008028.1:g.13922A=
NG_012954.1:g.407A=
NG_012954.2:g.442A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258385.8:c.1375A= MANE Select	ENSP00000258385.3:p.Lys459=
ENST00000258385.7:c.1375A=	ENSP00000258385.3:p.Lys459=
ENST00000441621.6:c.*557A=	ENSP00000408819.2:n.*557A=
ENST00000446616.1:c.*1016A=	ENSP00000410801.1:n.*1016A=
ENST00000543200.5:c.1330A=	ENSP00000438380.1:p.Lys444=
NM_000751.2:c.1375A=	NP_000742.1:p.Lys459=
NM_001256657.1:c.1330A=	NP_001243586.1:p.Lys444=
NM_001311195.1:c.793A=	NP_001298124.1:p.Lys265=
NM_001311196.1:c.1072A=	NP_001298125.1:p.Lys358=
NR_046333.1:c.-4294966176A=
NR_046334.1:c.-4294965897A=
XM_011510524.1:c.994A=	XP_011508826.1:p.Lys332=
XM_011510524.2:c.994A=	XP_011508826.1:p.Lys332=
NM_000751.3:c.1375A= MANE Select	NP_000742.1:p.Lys459=
NM_001311195.2:c.793A=	NP_001298124.1:p.Lys265=
NM_001311196.2:c.1072A=	NP_001298125.1:p.Lys358=
NM_001256657.2:c.1330A=	NP_001243586.1:p.Lys444=