Canonical Allele Identifier: CA351005816

Gene: CHRND

Linked Data

• COSMIC: COSM3414369
• MyVariant Identifiers: chr2:g.233399032G>C (hg19) ; chr2:g.232534322G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534322G>C , CM000664.2:g.232534322G>C	GRCh38
NC_000002.11:g.233399032G>C , CM000664.1:g.233399032G>C	GRCh37
NC_000002.10:g.233107276G>C	NCBI36
NG_008028.1:g.13111G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1351G>C MANE Select	ENSP00000258385.3:p.Asp451His
ENST00000258385.7:c.1351G>C	ENSP00000258385.3:p.Asp451His
ENST00000441621.6:c.*533G>C	ENSP00000408819.2:n.*533G>C
ENST00000446616.1:c.*992G>C	ENSP00000410801.1:n.*992G>C
ENST00000543200.5:c.1306G>C	ENSP00000438380.1:p.Asp436His
NM_000751.2:c.1351G>C	NP_000742.1:p.Asp451His
NM_001256657.1:c.1306G>C	NP_001243586.1:p.Asp436His
NM_001311195.1:c.769G>C	NP_001298124.1:p.Asp257His
NM_001311196.1:c.1048G>C	NP_001298125.1:p.Asp350His
NR_046333.1:c.-4294966200G>C
NR_046334.1:c.-4294965921G>C
XM_011510524.1:c.970G>C	XP_011508826.1:p.Asp324His
XM_011510524.2:c.970G>C	XP_011508826.1:p.Asp324His
NM_000751.3:c.1351G>C MANE Select	NP_000742.1:p.Asp451His
NM_001311195.2:c.769G>C	NP_001298124.1:p.Asp257His
NM_001311196.2:c.1048G>C	NP_001298125.1:p.Asp350His
NM_001256657.2:c.1306G>C	NP_001243586.1:p.Asp436His