Canonical Allele Identifier: CA1335310448

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232528360G= , CM000664.2:g.232528360G=	GRCh38
NC_000002.11:g.233393070G= , CM000664.1:g.233393070G=	GRCh37
NC_000002.10:g.233101314G=	NCBI36
NG_008028.1:g.7149G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.342G= MANE Select	ENSP00000258385.3:p.Val114=
ENST00000258385.7:c.342G=	ENSP00000258385.3:p.Val114=
ENST00000412233.5:c.342G=	ENSP00000398143.1:p.Val114=
ENST00000441621.6:c.342G=	ENSP00000408819.2:p.Val114=
ENST00000446616.1:c.321+21G=	ENSP00000410801.1:n.321+21G=
ENST00000449596.5:c.297G=	ENSP00000404950.1:p.Val99=
ENST00000543200.5:c.297G=	ENSP00000438380.1:p.Val99=
NM_000751.2:c.342G=	NP_000742.1:p.Val114=
NM_001256657.1:c.297G=	NP_001243586.1:p.Val99=
NM_001311195.1:c.71G=	NP_001298124.1:p.Cys24=
NM_001311196.1:c.50+21G=	NP_001298125.1:n.50+21G=
NR_046333.1:c.-4294966898G=
NR_046334.1:c.-4294966919+21G=
XM_011510524.1:c.71G=	XP_011508826.1:p.Cys24=
XM_011510524.2:c.71G=	XP_011508826.1:p.Cys24=
NM_000751.3:c.342G= MANE Select	NP_000742.1:p.Val114=
NM_001311195.2:c.71G=	NP_001298124.1:p.Cys24=
NM_001311196.2:c.50+21G=	NP_001298125.1:n.50+21G=
NM_001256657.2:c.297G=	NP_001243586.1:p.Val99=