Canonical Allele Identifier: CA1335314466

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232535141C= , CM000664.2:g.232535141C=	GRCh38
NC_000002.11:g.233399851C= , CM000664.1:g.233399851C=	GRCh37
NC_000002.10:g.233108095C=	NCBI36
NG_008028.1:g.13930C=
NG_012954.1:g.415C=
NG_012954.2:g.450C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258385.8:c.1383C= MANE Select	ENSP00000258385.3:p.Ser461=
ENST00000258385.7:c.1383C=	ENSP00000258385.3:p.Ser461=
ENST00000441621.6:c.*565C=	ENSP00000408819.2:n.*565C=
ENST00000446616.1:c.*1024C=	ENSP00000410801.1:n.*1024C=
ENST00000543200.5:c.1338C=	ENSP00000438380.1:p.Ser446=
NM_000751.2:c.1383C=	NP_000742.1:p.Ser461=
NM_001256657.1:c.1338C=	NP_001243586.1:p.Ser446=
NM_001311195.1:c.801C=	NP_001298124.1:p.Ser267=
NM_001311196.1:c.1080C=	NP_001298125.1:p.Ser360=
NR_046333.1:c.-4294966168C=
NR_046334.1:c.-4294965889C=
XM_011510524.1:c.1002C=	XP_011508826.1:p.Ser334=
XM_011510524.2:c.1002C=	XP_011508826.1:p.Ser334=
NM_000751.3:c.1383C= MANE Select	NP_000742.1:p.Ser461=
NM_001311195.2:c.801C=	NP_001298124.1:p.Ser267=
NM_001311196.2:c.1080C=	NP_001298125.1:p.Ser360=
NM_001256657.2:c.1338C=	NP_001243586.1:p.Ser446=