Canonical Allele Identifier: CA351005911

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233399852T>C (hg19) ; chr2:g.232535142T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232535142T>C , CM000664.2:g.232535142T>C	GRCh38
NC_000002.11:g.233399852T>C , CM000664.1:g.233399852T>C	GRCh37
NC_000002.10:g.233108096T>C	NCBI36
NG_008028.1:g.13931T>C
NG_012954.1:g.416T>C
NG_012954.2:g.451T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000258385.8:c.1384T>C MANE Select	ENSP00000258385.3:p.Trp462Arg
ENST00000258385.7:c.1384T>C	ENSP00000258385.3:p.Trp462Arg
ENST00000441621.6:c.*566T>C	ENSP00000408819.2:n.*566T>C
ENST00000446616.1:c.*1025T>C	ENSP00000410801.1:n.*1025T>C
ENST00000543200.5:c.1339T>C	ENSP00000438380.1:p.Trp447Arg
NM_000751.2:c.1384T>C	NP_000742.1:p.Trp462Arg
NM_001256657.1:c.1339T>C	NP_001243586.1:p.Trp447Arg
NM_001311195.1:c.802T>C	NP_001298124.1:p.Trp268Arg
NM_001311196.1:c.1081T>C	NP_001298125.1:p.Trp361Arg
NR_046333.1:c.-4294966167T>C
NR_046334.1:c.-4294965888T>C
XM_011510524.1:c.1003T>C	XP_011508826.1:p.Trp335Arg
XM_011510524.2:c.1003T>C	XP_011508826.1:p.Trp335Arg
NM_000751.3:c.1384T>C MANE Select	NP_000742.1:p.Trp462Arg
NM_001311195.2:c.802T>C	NP_001298124.1:p.Trp268Arg
NM_001311196.2:c.1081T>C	NP_001298125.1:p.Trp361Arg
NM_001256657.2:c.1339T>C	NP_001243586.1:p.Trp447Arg