Canonical Allele Identifier: CA1335314030

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534145C= , CM000664.2:g.232534145C=	GRCh38
NC_000002.11:g.233398855C= , CM000664.1:g.233398855C=	GRCh37
NC_000002.10:g.233107099C=	NCBI36
NG_008028.1:g.12934C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1252+10C= MANE Select	ENSP00000258385.3:n.1252+10C=
ENST00000258385.7:c.1252+10C=	ENSP00000258385.3:n.1252+10C=
ENST00000441621.6:c.*434+10C=	ENSP00000408819.2:n.*434+10C=
ENST00000446616.1:c.*893+10C=	ENSP00000410801.1:n.*893+10C=
ENST00000543200.5:c.1207+10C=	ENSP00000438380.1:n.1207+10C=
NM_000751.2:c.1252+10C=	NP_000742.1:n.1252+10C=
NM_001256657.1:c.1207+10C=	NP_001243586.1:n.1207+10C=
NM_001311195.1:c.670+10C=	NP_001298124.1:n.670+10C=
NM_001311196.1:c.949+10C=	NP_001298125.1:n.949+10C=
NR_046333.1:c.-4294966299+10C=
NR_046334.1:c.-4294966020+10C=
XM_011510524.1:c.871+10C=	XP_011508826.1:n.871+10C=
XM_011510524.2:c.871+10C=	XP_011508826.1:n.871+10C=
NM_000751.3:c.1252+10C= MANE Select	NP_000742.1:n.1252+10C=
NM_001311195.2:c.670+10C=	NP_001298124.1:n.670+10C=
NM_001311196.2:c.949+10C=	NP_001298125.1:n.949+10C=
NM_001256657.2:c.1207+10C=	NP_001243586.1:n.1207+10C=