Canonical Allele Identifier: CA351005840

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233399042A>C (hg19) ; chr2:g.232534332A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534332A>C , CM000664.2:g.232534332A>C	GRCh38
NC_000002.11:g.233399042A>C , CM000664.1:g.233399042A>C	GRCh37
NC_000002.10:g.233107286A>C	NCBI36
NG_008028.1:g.13121A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1361A>C MANE Select	ENSP00000258385.3:p.Asn454Thr
ENST00000258385.7:c.1361A>C	ENSP00000258385.3:p.Asn454Thr
ENST00000441621.6:c.*543A>C	ENSP00000408819.2:n.*543A>C
ENST00000446616.1:c.*1002A>C	ENSP00000410801.1:n.*1002A>C
ENST00000543200.5:c.1316A>C	ENSP00000438380.1:p.Asn439Thr
NM_000751.2:c.1361A>C	NP_000742.1:p.Asn454Thr
NM_001256657.1:c.1316A>C	NP_001243586.1:p.Asn439Thr
NM_001311195.1:c.779A>C	NP_001298124.1:p.Asn260Thr
NM_001311196.1:c.1058A>C	NP_001298125.1:p.Asn353Thr
NR_046333.1:c.-4294966190A>C
NR_046334.1:c.-4294965911A>C
XM_011510524.1:c.980A>C	XP_011508826.1:p.Asn327Thr
XM_011510524.2:c.980A>C	XP_011508826.1:p.Asn327Thr
NM_000751.3:c.1361A>C MANE Select	NP_000742.1:p.Asn454Thr
NM_001311195.2:c.779A>C	NP_001298124.1:p.Asn260Thr
NM_001311196.2:c.1058A>C	NP_001298125.1:p.Asn353Thr
NM_001256657.2:c.1316A>C	NP_001243586.1:p.Asn439Thr