Canonical Allele Identifier: CA1335314079

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534250G= , CM000664.2:g.232534250G=	GRCh38
NC_000002.11:g.233398960G= , CM000664.1:g.233398960G=	GRCh37
NC_000002.10:g.233107204G=	NCBI36
NG_008028.1:g.13039G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1279G= MANE Select	ENSP00000258385.3:p.Ala427=
ENST00000258385.7:c.1279G=	ENSP00000258385.3:p.Ala427=
ENST00000441621.6:c.*461G=	ENSP00000408819.2:n.*461G=
ENST00000446616.1:c.*920G=	ENSP00000410801.1:n.*920G=
ENST00000543200.5:c.1234G=	ENSP00000438380.1:p.Ala412=
NM_000751.2:c.1279G=	NP_000742.1:p.Ala427=
NM_001256657.1:c.1234G=	NP_001243586.1:p.Ala412=
NM_001311195.1:c.697G=	NP_001298124.1:p.Ala233=
NM_001311196.1:c.976G=	NP_001298125.1:p.Ala326=
NR_046333.1:c.-4294966272G=
NR_046334.1:c.-4294965993G=
XM_011510524.1:c.898G=	XP_011508826.1:p.Ala300=
XM_011510524.2:c.898G=	XP_011508826.1:p.Ala300=
NM_000751.3:c.1279G= MANE Select	NP_000742.1:p.Ala427=
NM_001311195.2:c.697G=	NP_001298124.1:p.Ala233=
NM_001311196.2:c.976G=	NP_001298125.1:p.Ala326=
NM_001256657.2:c.1234G=	NP_001243586.1:p.Ala412=