Canonical Allele Identifier: CA1335314131

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534392T= , CM000664.2:g.232534392T=	GRCh38
NC_000002.11:g.233399102T= , CM000664.1:g.233399102T=	GRCh37
NC_000002.10:g.233107346T=	NCBI36
NG_008028.1:g.13181T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1371+50T= MANE Select	ENSP00000258385.3:n.1371+50T=
ENST00000258385.7:c.1371+50T=	ENSP00000258385.3:n.1371+50T=
ENST00000441621.6:c.*553+50T=	ENSP00000408819.2:n.*553+50T=
ENST00000446616.1:c.*1012+50T=	ENSP00000410801.1:n.*1012+50T=
ENST00000543200.5:c.1326+50T=	ENSP00000438380.1:n.1326+50T=
NM_000751.2:c.1371+50T=	NP_000742.1:n.1371+50T=
NM_001256657.1:c.1326+50T=	NP_001243586.1:n.1326+50T=
NM_001311195.1:c.789+50T=	NP_001298124.1:n.789+50T=
NM_001311196.1:c.1068+50T=	NP_001298125.1:n.1068+50T=
NR_046333.1:c.-4294966180+50T=
NR_046334.1:c.-4294965901+50T=
XM_011510524.1:c.990+50T=	XP_011508826.1:n.990+50T=
XM_011510524.2:c.990+50T=	XP_011508826.1:n.990+50T=
NM_000751.3:c.1371+50T= MANE Select	NP_000742.1:n.1371+50T=
NM_001311195.2:c.789+50T=	NP_001298124.1:n.789+50T=
NM_001311196.2:c.1068+50T=	NP_001298125.1:n.1068+50T=
NM_001256657.2:c.1326+50T=	NP_001243586.1:n.1326+50T=