Canonical Allele Identifier: CA350997540

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233393050G>A (hg19) ; chr2:g.232528340G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232528340G>A , CM000664.2:g.232528340G>A	GRCh38
NC_000002.11:g.233393050G>A , CM000664.1:g.233393050G>A	GRCh37
NC_000002.10:g.233101294G>A	NCBI36
NG_008028.1:g.7129G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.322G>A MANE Select	ENSP00000258385.3:p.Val108Met
ENST00000258385.7:c.322G>A	ENSP00000258385.3:p.Val108Met
ENST00000412233.5:c.322G>A	ENSP00000398143.1:p.Val108Met
ENST00000441621.6:c.322G>A	ENSP00000408819.2:p.Val108Met
ENST00000446616.1:c.321+1G>A	ENSP00000410801.1:n.321+1G>A
ENST00000449596.5:c.277G>A	ENSP00000404950.1:p.Val93Met
ENST00000543200.5:c.277G>A	ENSP00000438380.1:p.Val93Met
NM_000751.2:c.322G>A	NP_000742.1:p.Val108Met
NM_001256657.1:c.277G>A	NP_001243586.1:p.Val93Met
NM_001311195.1:c.51G>A	NP_001298124.1:p.Trp17Ter
NM_001311196.1:c.50+1G>A	NP_001298125.1:n.50+1G>A
NR_046333.1:c.-4294966918G>A
NR_046334.1:c.-4294966919+1G>A
XM_011510524.1:c.51G>A	XP_011508826.1:p.Trp17Ter
XM_011510524.2:c.51G>A	XP_011508826.1:p.Trp17Ter
NM_000751.3:c.322G>A MANE Select	NP_000742.1:p.Val108Met
NM_001311195.2:c.51G>A	NP_001298124.1:p.Trp17Ter
NM_001311196.2:c.50+1G>A	NP_001298125.1:n.50+1G>A
NM_001256657.2:c.277G>A	NP_001243586.1:p.Val93Met