Canonical Allele Identifier: CA1335314011

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534106A= , CM000664.2:g.232534106A=	GRCh38
NC_000002.11:g.233398816A= , CM000664.1:g.233398816A=	GRCh37
NC_000002.10:g.233107060A=	NCBI36
NG_008028.1:g.12895A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1223A= MANE Select	ENSP00000258385.3:p.His408=
ENST00000258385.7:c.1223A=	ENSP00000258385.3:p.His408=
ENST00000441621.6:c.*405A=	ENSP00000408819.2:n.*405A=
ENST00000446616.1:c.*864A=	ENSP00000410801.1:n.*864A=
ENST00000543200.5:c.1178A=	ENSP00000438380.1:p.His393=
NM_000751.2:c.1223A=	NP_000742.1:p.His408=
NM_001256657.1:c.1178A=	NP_001243586.1:p.His393=
NM_001311195.1:c.641A=	NP_001298124.1:p.His214=
NM_001311196.1:c.920A=	NP_001298125.1:p.His307=
NR_046333.1:c.-4294966328A=
NR_046334.1:c.-4294966049A=
XM_011510524.1:c.842A=	XP_011508826.1:p.His281=
XM_011510524.2:c.842A=	XP_011508826.1:p.His281=
NM_000751.3:c.1223A= MANE Select	NP_000742.1:p.His408=
NM_001311195.2:c.641A=	NP_001298124.1:p.His214=
NM_001311196.2:c.920A=	NP_001298125.1:p.His307=
NM_001256657.2:c.1178A=	NP_001243586.1:p.His393=