Canonical Allele Identifier: CA1335314091

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534279G= , CM000664.2:g.232534279G=	GRCh38
NC_000002.11:g.233398989G= , CM000664.1:g.233398989G=	GRCh37
NC_000002.10:g.233107233G=	NCBI36
NG_008028.1:g.13068G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1308G= MANE Select	ENSP00000258385.3:p.Lys436=
ENST00000258385.7:c.1308G=	ENSP00000258385.3:p.Lys436=
ENST00000441621.6:c.*490G=	ENSP00000408819.2:n.*490G=
ENST00000446616.1:c.*949G=	ENSP00000410801.1:n.*949G=
ENST00000543200.5:c.1263G=	ENSP00000438380.1:p.Lys421=
NM_000751.2:c.1308G=	NP_000742.1:p.Lys436=
NM_001256657.1:c.1263G=	NP_001243586.1:p.Lys421=
NM_001311195.1:c.726G=	NP_001298124.1:p.Lys242=
NM_001311196.1:c.1005G=	NP_001298125.1:p.Lys335=
NR_046333.1:c.-4294966243G=
NR_046334.1:c.-4294965964G=
XM_011510524.1:c.927G=	XP_011508826.1:p.Lys309=
XM_011510524.2:c.927G=	XP_011508826.1:p.Lys309=
NM_000751.3:c.1308G= MANE Select	NP_000742.1:p.Lys436=
NM_001311195.2:c.726G=	NP_001298124.1:p.Lys242=
NM_001311196.2:c.1005G=	NP_001298125.1:p.Lys335=
NM_001256657.2:c.1263G=	NP_001243586.1:p.Lys421=