Canonical Allele Identifier: CA431952538

Gene: CHRND

Linked Data

• dbSNP Id: rs1277179506
• gnomAD v2: 2-233398757-G-A
• MyVariant Identifiers: chr2:g.233398757G>A (hg19) ; chr2:g.232534047G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534047G>A , CM000664.2:g.232534047G>A	GRCh38
NC_000002.11:g.233398757G>A , CM000664.1:g.233398757G>A	GRCh37
NC_000002.10:g.233107001G>A	NCBI36
NG_008028.1:g.12836G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1164G>A MANE Select	ENSP00000258385.3:p.Glu388=
ENST00000258385.7:c.1164G>A	ENSP00000258385.3:p.Glu388=
ENST00000441621.6:c.*346G>A	ENSP00000408819.2:n.*346G>A
ENST00000446616.1:c.*805G>A	ENSP00000410801.1:n.*805G>A
ENST00000543200.5:c.1119G>A	ENSP00000438380.1:p.Glu373=
NM_000751.2:c.1164G>A	NP_000742.1:p.Glu388=
NM_001256657.1:c.1119G>A	NP_001243586.1:p.Glu373=
NM_001311195.1:c.582G>A	NP_001298124.1:p.Glu194=
NM_001311196.1:c.861G>A	NP_001298125.1:p.Glu287=
NR_046333.1:c.-4294966387G>A
NR_046334.1:c.-4294966108G>A
XM_011510524.1:c.783G>A	XP_011508826.1:p.Glu261=
XM_011510524.2:c.783G>A	XP_011508826.1:p.Glu261=
NM_000751.3:c.1164G>A MANE Select	NP_000742.1:p.Glu388=
NM_001311195.2:c.582G>A	NP_001298124.1:p.Glu194=
NM_001311196.2:c.861G>A	NP_001298125.1:p.Glu287=
NM_001256657.2:c.1119G>A	NP_001243586.1:p.Glu373=