Canonical Allele Identifier: CA1335314083

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534257A= , CM000664.2:g.232534257A=	GRCh38
NC_000002.11:g.233398967A= , CM000664.1:g.233398967A=	GRCh37
NC_000002.10:g.233107211A=	NCBI36
NG_008028.1:g.13046A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1286A= MANE Select	ENSP00000258385.3:p.Gln429=
ENST00000258385.7:c.1286A=	ENSP00000258385.3:p.Gln429=
ENST00000441621.6:c.*468A=	ENSP00000408819.2:n.*468A=
ENST00000446616.1:c.*927A=	ENSP00000410801.1:n.*927A=
ENST00000543200.5:c.1241A=	ENSP00000438380.1:p.Gln414=
NM_000751.2:c.1286A=	NP_000742.1:p.Gln429=
NM_001256657.1:c.1241A=	NP_001243586.1:p.Gln414=
NM_001311195.1:c.704A=	NP_001298124.1:p.Gln235=
NM_001311196.1:c.983A=	NP_001298125.1:p.Gln328=
NR_046333.1:c.-4294966265A=
NR_046334.1:c.-4294965986A=
XM_011510524.1:c.905A=	XP_011508826.1:p.Gln302=
XM_011510524.2:c.905A=	XP_011508826.1:p.Gln302=
NM_000751.3:c.1286A= MANE Select	NP_000742.1:p.Gln429=
NM_001311195.2:c.704A=	NP_001298124.1:p.Gln235=
NM_001311196.2:c.983A=	NP_001298125.1:p.Gln328=
NM_001256657.2:c.1241A=	NP_001243586.1:p.Gln414=