Canonical Allele Identifier: CA1335310427

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232528313A= , CM000664.2:g.232528313A=	GRCh38
NC_000002.11:g.233393023A= , CM000664.1:g.233393023A=	GRCh37
NC_000002.10:g.233101267A=	NCBI36
NG_008028.1:g.7102A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.295A= MANE Select	ENSP00000258385.3:p.Ser99=
ENST00000258385.7:c.295A=	ENSP00000258385.3:p.Ser99=
ENST00000412233.5:c.295A=	ENSP00000398143.1:p.Ser99=
ENST00000441621.6:c.295A=	ENSP00000408819.2:p.Ser99=
ENST00000446616.1:c.295A=	ENSP00000410801.1:p.Ser99=
ENST00000449596.5:c.250A=	ENSP00000404950.1:p.Ser84=
ENST00000543200.5:c.250A=	ENSP00000438380.1:p.Ser84=
NM_000751.2:c.295A=	NP_000742.1:p.Ser99=
NM_001256657.1:c.250A=	NP_001243586.1:p.Ser84=
NM_001311195.1:c.24A=	NP_001298124.1:p.Ser8=
NM_001311196.1:c.24A=	NP_001298125.1:p.Ser8=
NR_046333.1:c.-4294966945A=
NR_046334.1:c.-4294966945A=
XM_011510524.1:c.24A=	XP_011508826.1:p.Ser8=
XM_011510524.2:c.24A=	XP_011508826.1:p.Ser8=
NM_000751.3:c.295A= MANE Select	NP_000742.1:p.Ser99=
NM_001311195.2:c.24A=	NP_001298124.1:p.Ser8=
NM_001311196.2:c.24A=	NP_001298125.1:p.Ser8=
NM_001256657.2:c.250A=	NP_001243586.1:p.Ser84=