Canonical Allele Identifier: CA351005263

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233398803C>T (hg19) ; chr2:g.232534093C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534093C>T , CM000664.2:g.232534093C>T	GRCh38
NC_000002.11:g.233398803C>T , CM000664.1:g.233398803C>T	GRCh37
NC_000002.10:g.233107047C>T	NCBI36
NG_008028.1:g.12882C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000258385.8:c.1210C>T MANE Select	ENSP00000258385.3:p.Gln404Ter
ENST00000258385.7:c.1210C>T	ENSP00000258385.3:p.Gln404Ter
ENST00000441621.6:c.*392C>T	ENSP00000408819.2:n.*392C>T
ENST00000446616.1:c.*851C>T	ENSP00000410801.1:n.*851C>T
ENST00000543200.5:c.1165C>T	ENSP00000438380.1:p.Gln389Ter
NM_000751.2:c.1210C>T	NP_000742.1:p.Gln404Ter
NM_001256657.1:c.1165C>T	NP_001243586.1:p.Gln389Ter
NM_001311195.1:c.628C>T	NP_001298124.1:p.Gln210Ter
NM_001311196.1:c.907C>T	NP_001298125.1:p.Gln303Ter
NR_046333.1:c.-4294966341C>T
NR_046334.1:c.-4294966062C>T
XM_011510524.1:c.829C>T	XP_011508826.1:p.Gln277Ter
XM_011510524.2:c.829C>T	XP_011508826.1:p.Gln277Ter
NM_000751.3:c.1210C>T MANE Select	NP_000742.1:p.Gln404Ter
NM_001311195.2:c.628C>T	NP_001298124.1:p.Gln210Ter
NM_001311196.2:c.907C>T	NP_001298125.1:p.Gln303Ter
NM_001256657.2:c.1165C>T	NP_001243586.1:p.Gln389Ter