Canonical Allele Identifier: CA1335313982

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534041G= , CM000664.2:g.232534041G=	GRCh38
NC_000002.11:g.233398751G= , CM000664.1:g.233398751G=	GRCh37
NC_000002.10:g.233106995G=	NCBI36
NG_008028.1:g.12830G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1158G= MANE Select	ENSP00000258385.3:p.Lys386=
ENST00000258385.7:c.1158G=	ENSP00000258385.3:p.Lys386=
ENST00000441621.6:c.*340G=	ENSP00000408819.2:n.*340G=
ENST00000446616.1:c.*799G=	ENSP00000410801.1:n.*799G=
ENST00000543200.5:c.1113G=	ENSP00000438380.1:p.Lys371=
NM_000751.2:c.1158G=	NP_000742.1:p.Lys386=
NM_001256657.1:c.1113G=	NP_001243586.1:p.Lys371=
NM_001311195.1:c.576G=	NP_001298124.1:p.Lys192=
NM_001311196.1:c.855G=	NP_001298125.1:p.Lys285=
NR_046333.1:c.-4294966393G=
NR_046334.1:c.-4294966114G=
XM_011510524.1:c.777G=	XP_011508826.1:p.Lys259=
XM_011510524.2:c.777G=	XP_011508826.1:p.Lys259=
NM_000751.3:c.1158G= MANE Select	NP_000742.1:p.Lys386=
NM_001311195.2:c.576G=	NP_001298124.1:p.Lys192=
NM_001311196.2:c.855G=	NP_001298125.1:p.Lys285=
NM_001256657.2:c.1113G=	NP_001243586.1:p.Lys371=