Canonical Allele Identifier: CA1335314092

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534281C= , CM000664.2:g.232534281C=	GRCh38
NC_000002.11:g.233398991C= , CM000664.1:g.233398991C=	GRCh37
NC_000002.10:g.233107235C=	NCBI36
NG_008028.1:g.13070C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1310C= MANE Select	ENSP00000258385.3:p.Pro437=
ENST00000258385.7:c.1310C=	ENSP00000258385.3:p.Pro437=
ENST00000441621.6:c.*492C=	ENSP00000408819.2:n.*492C=
ENST00000446616.1:c.*951C=	ENSP00000410801.1:n.*951C=
ENST00000543200.5:c.1265C=	ENSP00000438380.1:p.Pro422=
NM_000751.2:c.1310C=	NP_000742.1:p.Pro437=
NM_001256657.1:c.1265C=	NP_001243586.1:p.Pro422=
NM_001311195.1:c.728C=	NP_001298124.1:p.Pro243=
NM_001311196.1:c.1007C=	NP_001298125.1:p.Pro336=
NR_046333.1:c.-4294966241C=
NR_046334.1:c.-4294965962C=
XM_011510524.1:c.929C=	XP_011508826.1:p.Pro310=
XM_011510524.2:c.929C=	XP_011508826.1:p.Pro310=
NM_000751.3:c.1310C= MANE Select	NP_000742.1:p.Pro437=
NM_001311195.2:c.728C=	NP_001298124.1:p.Pro243=
NM_001311196.2:c.1007C=	NP_001298125.1:p.Pro336=
NM_001256657.2:c.1265C=	NP_001243586.1:p.Pro422=