Canonical Allele Identifier: CA1335314068

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534219T= , CM000664.2:g.232534219T=	GRCh38
NC_000002.11:g.233398929T= , CM000664.1:g.233398929T=	GRCh37
NC_000002.10:g.233107173T=	NCBI36
NG_008028.1:g.13008T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1253-5T= MANE Select	ENSP00000258385.3:n.1253-5T=
ENST00000258385.7:c.1253-5T=	ENSP00000258385.3:n.1253-5T=
ENST00000441621.6:c.*435-5T=	ENSP00000408819.2:n.*435-5T=
ENST00000446616.1:c.*894-5T=	ENSP00000410801.1:n.*894-5T=
ENST00000543200.5:c.1208-5T=	ENSP00000438380.1:n.1208-5T=
NM_000751.2:c.1253-5T=	NP_000742.1:n.1253-5T=
NM_001256657.1:c.1208-5T=	NP_001243586.1:n.1208-5T=
NM_001311195.1:c.671-5T=	NP_001298124.1:n.671-5T=
NM_001311196.1:c.950-5T=	NP_001298125.1:n.950-5T=
NR_046333.1:c.-4294966298-5T=
NR_046334.1:c.-4294966019-5T=
XM_011510524.1:c.872-5T=	XP_011508826.1:n.872-5T=
XM_011510524.2:c.872-5T=	XP_011508826.1:n.872-5T=
NM_000751.3:c.1253-5T= MANE Select	NP_000742.1:n.1253-5T=
NM_001311195.2:c.671-5T=	NP_001298124.1:n.671-5T=
NM_001311196.2:c.950-5T=	NP_001298125.1:n.950-5T=
NM_001256657.2:c.1208-5T=	NP_001243586.1:n.1208-5T=