Canonical Allele Identifier: CA1335313991

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534064A= , CM000664.2:g.232534064A=	GRCh38
NC_000002.11:g.233398774A= , CM000664.1:g.233398774A=	GRCh37
NC_000002.10:g.233107018A=	NCBI36
NG_008028.1:g.12853A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1181A= MANE Select	ENSP00000258385.3:p.Lys394=
ENST00000258385.7:c.1181A=	ENSP00000258385.3:p.Lys394=
ENST00000441621.6:c.*363A=	ENSP00000408819.2:n.*363A=
ENST00000446616.1:c.*822A=	ENSP00000410801.1:n.*822A=
ENST00000543200.5:c.1136A=	ENSP00000438380.1:p.Lys379=
NM_000751.2:c.1181A=	NP_000742.1:p.Lys394=
NM_001256657.1:c.1136A=	NP_001243586.1:p.Lys379=
NM_001311195.1:c.599A=	NP_001298124.1:p.Lys200=
NM_001311196.1:c.878A=	NP_001298125.1:p.Lys293=
NR_046333.1:c.-4294966370A=
NR_046334.1:c.-4294966091A=
XM_011510524.1:c.800A=	XP_011508826.1:p.Lys267=
XM_011510524.2:c.800A=	XP_011508826.1:p.Lys267=
NM_000751.3:c.1181A= MANE Select	NP_000742.1:p.Lys394=
NM_001311195.2:c.599A=	NP_001298124.1:p.Lys200=
NM_001311196.2:c.878A=	NP_001298125.1:p.Lys293=
NM_001256657.2:c.1136A=	NP_001243586.1:p.Lys379=