Canonical Allele Identifier: CA1335313999

Gene: CHRND

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534082T= , CM000664.2:g.232534082T=	GRCh38
NC_000002.11:g.233398792T= , CM000664.1:g.233398792T=	GRCh37
NC_000002.10:g.233107036T=	NCBI36
NG_008028.1:g.12871T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1199T= MANE Select	ENSP00000258385.3:p.Met400=
ENST00000258385.7:c.1199T=	ENSP00000258385.3:p.Met400=
ENST00000441621.6:c.*381T=	ENSP00000408819.2:n.*381T=
ENST00000446616.1:c.*840T=	ENSP00000410801.1:n.*840T=
ENST00000543200.5:c.1154T=	ENSP00000438380.1:p.Met385=
NM_000751.2:c.1199T=	NP_000742.1:p.Met400=
NM_001256657.1:c.1154T=	NP_001243586.1:p.Met385=
NM_001311195.1:c.617T=	NP_001298124.1:p.Met206=
NM_001311196.1:c.896T=	NP_001298125.1:p.Met299=
NR_046333.1:c.-4294966352T=
NR_046334.1:c.-4294966073T=
XM_011510524.1:c.818T=	XP_011508826.1:p.Met273=
XM_011510524.2:c.818T=	XP_011508826.1:p.Met273=
NM_000751.3:c.1199T= MANE Select	NP_000742.1:p.Met400=
NM_001311195.2:c.617T=	NP_001298124.1:p.Met206=
NM_001311196.2:c.896T=	NP_001298125.1:p.Met299=
NM_001256657.2:c.1154T=	NP_001243586.1:p.Met385=