Canonical Allele Identifier: CA1335310518

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232528501C= , CM000664.2:g.232528501C=	GRCh38
NC_000002.11:g.233393211C= , CM000664.1:g.233393211C=	GRCh37
NC_000002.10:g.233101455C=	NCBI36
NG_008028.1:g.7290C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.354C= MANE Select	ENSP00000258385.3:p.Asn118=
ENST00000258385.7:c.354C=	ENSP00000258385.3:p.Asn118=
ENST00000412233.5:c.354C=	ENSP00000398143.1:p.Asn118=
ENST00000441621.6:c.354C=	ENSP00000408819.2:p.Asn118=
ENST00000446616.1:c.322C=	ENSP00000410801.1:p.Gln108=
ENST00000449596.5:c.309C=	ENSP00000404950.1:p.Asn103=
ENST00000543200.5:c.309C=	ENSP00000438380.1:p.Asn103=
NM_000751.2:c.354C=	NP_000742.1:p.Asn118=
NM_001256657.1:c.309C=	NP_001243586.1:p.Asn103=
NM_001311195.1:c.83C=	NP_001298124.1:p.Thr28=
NM_001311196.1:c.51C=	NP_001298125.1:p.Cys17=
NR_046333.1:c.-4294966886C=
NR_046334.1:c.-4294966918C=
XM_011510524.1:c.83C=	XP_011508826.1:p.Thr28=
XM_011510524.2:c.83C=	XP_011508826.1:p.Thr28=
NM_000751.3:c.354C= MANE Select	NP_000742.1:p.Asn118=
NM_001311195.2:c.83C=	NP_001298124.1:p.Thr28=
NM_001311196.2:c.51C=	NP_001298125.1:p.Cys17=
NM_001256657.2:c.309C=	NP_001243586.1:p.Asn103=