Canonical Allele Identifier: CA431952518

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233398722A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534012A>C , CM000664.2:g.232534012A>C	GRCh38
NC_000002.11:g.233398722A>C , CM000664.1:g.233398722A>C	GRCh37
NC_000002.10:g.233106966A>C	NCBI36
NG_008028.1:g.12801A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1129A>C MANE Select	ENSP00000258385.3:p.Arg377=
ENST00000258385.7:c.1129A>C	ENSP00000258385.3:p.Arg377=
ENST00000441621.6:c.*311A>C	ENSP00000408819.2:n.*311A>C
ENST00000446616.1:c.*770A>C	ENSP00000410801.1:n.*770A>C
ENST00000543200.5:c.1084A>C	ENSP00000438380.1:p.Arg362=
NM_000751.2:c.1129A>C	NP_000742.1:p.Arg377=
NM_001256657.1:c.1084A>C	NP_001243586.1:p.Arg362=
NM_001311195.1:c.547A>C	NP_001298124.1:p.Arg183=
NM_001311196.1:c.826A>C	NP_001298125.1:p.Arg276=
NR_046333.1:c.-4294966422A>C
NR_046334.1:c.-4294966143A>C
XM_011510524.1:c.748A>C	XP_011508826.1:p.Arg250=
XM_011510524.2:c.748A>C	XP_011508826.1:p.Arg250=
NM_000751.3:c.1129A>C MANE Select	NP_000742.1:p.Arg377=
NM_001311195.2:c.547A>C	NP_001298124.1:p.Arg183=
NM_001311196.2:c.826A>C	NP_001298125.1:p.Arg276=
NM_001256657.2:c.1084A>C	NP_001243586.1:p.Arg362=