Canonical Allele Identifier: CA1335314032

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534148T= , CM000664.2:g.232534148T=	GRCh38
NC_000002.11:g.233398858T= , CM000664.1:g.233398858T=	GRCh37
NC_000002.10:g.233107102T=	NCBI36
NG_008028.1:g.12937T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1252+13T= MANE Select	ENSP00000258385.3:n.1252+13T=
ENST00000258385.7:c.1252+13T=	ENSP00000258385.3:n.1252+13T=
ENST00000441621.6:c.*434+13T=	ENSP00000408819.2:n.*434+13T=
ENST00000446616.1:c.*893+13T=	ENSP00000410801.1:n.*893+13T=
ENST00000543200.5:c.1207+13T=	ENSP00000438380.1:n.1207+13T=
NM_000751.2:c.1252+13T=	NP_000742.1:n.1252+13T=
NM_001256657.1:c.1207+13T=	NP_001243586.1:n.1207+13T=
NM_001311195.1:c.670+13T=	NP_001298124.1:n.670+13T=
NM_001311196.1:c.949+13T=	NP_001298125.1:n.949+13T=
NR_046333.1:c.-4294966299+13T=
NR_046334.1:c.-4294966020+13T=
XM_011510524.1:c.871+13T=	XP_011508826.1:n.871+13T=
XM_011510524.2:c.871+13T=	XP_011508826.1:n.871+13T=
NM_000751.3:c.1252+13T= MANE Select	NP_000742.1:n.1252+13T=
NM_001311195.2:c.670+13T=	NP_001298124.1:n.670+13T=
NM_001311196.2:c.949+13T=	NP_001298125.1:n.949+13T=
NM_001256657.2:c.1207+13T=	NP_001243586.1:n.1207+13T=