Canonical Allele Identifier: CA1335314105

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534327G= , CM000664.2:g.232534327G=	GRCh38
NC_000002.11:g.233399037G= , CM000664.1:g.233399037G=	GRCh37
NC_000002.10:g.233107281G=	NCBI36
NG_008028.1:g.13116G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1356G= MANE Select	ENSP00000258385.3:p.Gln452=
ENST00000258385.7:c.1356G=	ENSP00000258385.3:p.Gln452=
ENST00000441621.6:c.*538G=	ENSP00000408819.2:n.*538G=
ENST00000446616.1:c.*997G=	ENSP00000410801.1:n.*997G=
ENST00000543200.5:c.1311G=	ENSP00000438380.1:p.Gln437=
NM_000751.2:c.1356G=	NP_000742.1:p.Gln452=
NM_001256657.1:c.1311G=	NP_001243586.1:p.Gln437=
NM_001311195.1:c.774G=	NP_001298124.1:p.Gln258=
NM_001311196.1:c.1053G=	NP_001298125.1:p.Gln351=
NR_046333.1:c.-4294966195G=
NR_046334.1:c.-4294965916G=
XM_011510524.1:c.975G=	XP_011508826.1:p.Gln325=
XM_011510524.2:c.975G=	XP_011508826.1:p.Gln325=
NM_000751.3:c.1356G= MANE Select	NP_000742.1:p.Gln452=
NM_001311195.2:c.774G=	NP_001298124.1:p.Gln258=
NM_001311196.2:c.1053G=	NP_001298125.1:p.Gln351=
NM_001256657.2:c.1311G=	NP_001243586.1:p.Gln437=