Canonical Allele Identifier: CA1335313969

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534007T= , CM000664.2:g.232534007T=	GRCh38
NC_000002.11:g.233398717T= , CM000664.1:g.233398717T=	GRCh37
NC_000002.10:g.233106961T=	NCBI36
NG_008028.1:g.12796T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1124T= MANE Select	ENSP00000258385.3:p.Val375=
ENST00000258385.7:c.1124T=	ENSP00000258385.3:p.Val375=
ENST00000441621.6:c.*306T=	ENSP00000408819.2:n.*306T=
ENST00000446616.1:c.*765T=	ENSP00000410801.1:n.*765T=
ENST00000543200.5:c.1079T=	ENSP00000438380.1:p.Val360=
NM_000751.2:c.1124T=	NP_000742.1:p.Val375=
NM_001256657.1:c.1079T=	NP_001243586.1:p.Val360=
NM_001311195.1:c.542T=	NP_001298124.1:p.Val181=
NM_001311196.1:c.821T=	NP_001298125.1:p.Val274=
NR_046333.1:c.-4294966427T=
NR_046334.1:c.-4294966148T=
XM_011510524.1:c.743T=	XP_011508826.1:p.Val248=
XM_011510524.2:c.743T=	XP_011508826.1:p.Val248=
NM_000751.3:c.1124T= MANE Select	NP_000742.1:p.Val375=
NM_001311195.2:c.542T=	NP_001298124.1:p.Val181=
NM_001311196.2:c.821T=	NP_001298125.1:p.Val274=
NM_001256657.2:c.1079T=	NP_001243586.1:p.Val360=