Canonical Allele Identifier: CA1335314001

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534084T= , CM000664.2:g.232534084T=	GRCh38
NC_000002.11:g.233398794T= , CM000664.1:g.233398794T=	GRCh37
NC_000002.10:g.233107038T=	NCBI36
NG_008028.1:g.12873T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1201T= MANE Select	ENSP00000258385.3:p.Phe401=
ENST00000258385.7:c.1201T=	ENSP00000258385.3:p.Phe401=
ENST00000441621.6:c.*383T=	ENSP00000408819.2:n.*383T=
ENST00000446616.1:c.*842T=	ENSP00000410801.1:n.*842T=
ENST00000543200.5:c.1156T=	ENSP00000438380.1:p.Phe386=
NM_000751.2:c.1201T=	NP_000742.1:p.Phe401=
NM_001256657.1:c.1156T=	NP_001243586.1:p.Phe386=
NM_001311195.1:c.619T=	NP_001298124.1:p.Phe207=
NM_001311196.1:c.898T=	NP_001298125.1:p.Phe300=
NR_046333.1:c.-4294966350T=
NR_046334.1:c.-4294966071T=
XM_011510524.1:c.820T=	XP_011508826.1:p.Phe274=
XM_011510524.2:c.820T=	XP_011508826.1:p.Phe274=
NM_000751.3:c.1201T= MANE Select	NP_000742.1:p.Phe401=
NM_001311195.2:c.619T=	NP_001298124.1:p.Phe207=
NM_001311196.2:c.898T=	NP_001298125.1:p.Phe300=
NM_001256657.2:c.1156T=	NP_001243586.1:p.Phe386=