Canonical Allele Identifier: CA1335314123

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534372G= , CM000664.2:g.232534372G=	GRCh38
NC_000002.11:g.233399082G= , CM000664.1:g.233399082G=	GRCh37
NC_000002.10:g.233107326G=	NCBI36
NG_008028.1:g.13161G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1371+30G= MANE Select	ENSP00000258385.3:n.1371+30G=
ENST00000258385.7:c.1371+30G=	ENSP00000258385.3:n.1371+30G=
ENST00000441621.6:c.*553+30G=	ENSP00000408819.2:n.*553+30G=
ENST00000446616.1:c.*1012+30G=	ENSP00000410801.1:n.*1012+30G=
ENST00000543200.5:c.1326+30G=	ENSP00000438380.1:n.1326+30G=
NM_000751.2:c.1371+30G=	NP_000742.1:n.1371+30G=
NM_001256657.1:c.1326+30G=	NP_001243586.1:n.1326+30G=
NM_001311195.1:c.789+30G=	NP_001298124.1:n.789+30G=
NM_001311196.1:c.1068+30G=	NP_001298125.1:n.1068+30G=
NR_046333.1:c.-4294966180+30G=
NR_046334.1:c.-4294965901+30G=
XM_011510524.1:c.990+30G=	XP_011508826.1:n.990+30G=
XM_011510524.2:c.990+30G=	XP_011508826.1:n.990+30G=
NM_000751.3:c.1371+30G= MANE Select	NP_000742.1:n.1371+30G=
NM_001311195.2:c.789+30G=	NP_001298124.1:n.789+30G=
NM_001311196.2:c.1068+30G=	NP_001298125.1:n.1068+30G=
NM_001256657.2:c.1326+30G=	NP_001243586.1:n.1326+30G=