Canonical Allele Identifier: CA1335314119

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534365T= , CM000664.2:g.232534365T=	GRCh38
NC_000002.11:g.233399075T= , CM000664.1:g.233399075T=	GRCh37
NC_000002.10:g.233107319T=	NCBI36
NG_008028.1:g.13154T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1371+23T= MANE Select	ENSP00000258385.3:n.1371+23T=
ENST00000258385.7:c.1371+23T=	ENSP00000258385.3:n.1371+23T=
ENST00000441621.6:c.*553+23T=	ENSP00000408819.2:n.*553+23T=
ENST00000446616.1:c.*1012+23T=	ENSP00000410801.1:n.*1012+23T=
ENST00000543200.5:c.1326+23T=	ENSP00000438380.1:n.1326+23T=
NM_000751.2:c.1371+23T=	NP_000742.1:n.1371+23T=
NM_001256657.1:c.1326+23T=	NP_001243586.1:n.1326+23T=
NM_001311195.1:c.789+23T=	NP_001298124.1:n.789+23T=
NM_001311196.1:c.1068+23T=	NP_001298125.1:n.1068+23T=
NR_046333.1:c.-4294966180+23T=
NR_046334.1:c.-4294965901+23T=
XM_011510524.1:c.990+23T=	XP_011508826.1:n.990+23T=
XM_011510524.2:c.990+23T=	XP_011508826.1:n.990+23T=
NM_000751.3:c.1371+23T= MANE Select	NP_000742.1:n.1371+23T=
NM_001311195.2:c.789+23T=	NP_001298124.1:n.789+23T=
NM_001311196.2:c.1068+23T=	NP_001298125.1:n.1068+23T=
NM_001256657.2:c.1326+23T=	NP_001243586.1:n.1326+23T=