Canonical Allele Identifier: CA1335314084

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534261A= , CM000664.2:g.232534261A=	GRCh38
NC_000002.11:g.233398971A= , CM000664.1:g.233398971A=	GRCh37
NC_000002.10:g.233107215A=	NCBI36
NG_008028.1:g.13050A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1290A= MANE Select	ENSP00000258385.3:p.Glu430=
ENST00000258385.7:c.1290A=	ENSP00000258385.3:p.Glu430=
ENST00000441621.6:c.*472A=	ENSP00000408819.2:n.*472A=
ENST00000446616.1:c.*931A=	ENSP00000410801.1:n.*931A=
ENST00000543200.5:c.1245A=	ENSP00000438380.1:p.Glu415=
NM_000751.2:c.1290A=	NP_000742.1:p.Glu430=
NM_001256657.1:c.1245A=	NP_001243586.1:p.Glu415=
NM_001311195.1:c.708A=	NP_001298124.1:p.Glu236=
NM_001311196.1:c.987A=	NP_001298125.1:p.Glu329=
NR_046333.1:c.-4294966261A=
NR_046334.1:c.-4294965982A=
XM_011510524.1:c.909A=	XP_011508826.1:p.Glu303=
XM_011510524.2:c.909A=	XP_011508826.1:p.Glu303=
NM_000751.3:c.1290A= MANE Select	NP_000742.1:p.Glu430=
NM_001311195.2:c.708A=	NP_001298124.1:p.Glu236=
NM_001311196.2:c.987A=	NP_001298125.1:p.Glu329=
NM_001256657.2:c.1245A=	NP_001243586.1:p.Glu415=