Canonical Allele Identifier: CA1335314086

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534266T= , CM000664.2:g.232534266T=	GRCh38
NC_000002.11:g.233398976T= , CM000664.1:g.233398976T=	GRCh37
NC_000002.10:g.233107220T=	NCBI36
NG_008028.1:g.13055T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1295T= MANE Select	ENSP00000258385.3:p.Phe432=
ENST00000258385.7:c.1295T=	ENSP00000258385.3:p.Phe432=
ENST00000441621.6:c.*477T=	ENSP00000408819.2:n.*477T=
ENST00000446616.1:c.*936T=	ENSP00000410801.1:n.*936T=
ENST00000543200.5:c.1250T=	ENSP00000438380.1:p.Phe417=
NM_000751.2:c.1295T=	NP_000742.1:p.Phe432=
NM_001256657.1:c.1250T=	NP_001243586.1:p.Phe417=
NM_001311195.1:c.713T=	NP_001298124.1:p.Phe238=
NM_001311196.1:c.992T=	NP_001298125.1:p.Phe331=
NR_046333.1:c.-4294966256T=
NR_046334.1:c.-4294965977T=
XM_011510524.1:c.914T=	XP_011508826.1:p.Phe305=
XM_011510524.2:c.914T=	XP_011508826.1:p.Phe305=
NM_000751.3:c.1295T= MANE Select	NP_000742.1:p.Phe432=
NM_001311195.2:c.713T=	NP_001298124.1:p.Phe238=
NM_001311196.2:c.992T=	NP_001298125.1:p.Phe331=
NM_001256657.2:c.1250T=	NP_001243586.1:p.Phe417=