Canonical Allele Identifier: CA351005759

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233399017G>A (hg19) ; chr2:g.232534307G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534307G>A , CM000664.2:g.232534307G>A	GRCh38
NC_000002.11:g.233399017G>A , CM000664.1:g.233399017G>A	GRCh37
NC_000002.10:g.233107261G>A	NCBI36
NG_008028.1:g.13096G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1336G>A MANE Select	ENSP00000258385.3:p.Val446Ile
ENST00000258385.7:c.1336G>A	ENSP00000258385.3:p.Val446Ile
ENST00000441621.6:c.*518G>A	ENSP00000408819.2:n.*518G>A
ENST00000446616.1:c.*977G>A	ENSP00000410801.1:n.*977G>A
ENST00000543200.5:c.1291G>A	ENSP00000438380.1:p.Val431Ile
NM_000751.2:c.1336G>A	NP_000742.1:p.Val446Ile
NM_001256657.1:c.1291G>A	NP_001243586.1:p.Val431Ile
NM_001311195.1:c.754G>A	NP_001298124.1:p.Val252Ile
NM_001311196.1:c.1033G>A	NP_001298125.1:p.Val345Ile
NR_046333.1:c.-4294966215G>A
NR_046334.1:c.-4294965936G>A
XM_011510524.1:c.955G>A	XP_011508826.1:p.Val319Ile
XM_011510524.2:c.955G>A	XP_011508826.1:p.Val319Ile
NM_000751.3:c.1336G>A MANE Select	NP_000742.1:p.Val446Ile
NM_001311195.2:c.754G>A	NP_001298124.1:p.Val252Ile
NM_001311196.2:c.1033G>A	NP_001298125.1:p.Val345Ile
NM_001256657.2:c.1291G>A	NP_001243586.1:p.Val431Ile