Canonical Allele Identifier: CA351005769

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233399018T>G (hg19) ; chr2:g.232534308T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534308T>G , CM000664.2:g.232534308T>G	GRCh38
NC_000002.11:g.233399018T>G , CM000664.1:g.233399018T>G	GRCh37
NC_000002.10:g.233107262T>G	NCBI36
NG_008028.1:g.13097T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1337T>G MANE Select	ENSP00000258385.3:p.Val446Gly
ENST00000258385.7:c.1337T>G	ENSP00000258385.3:p.Val446Gly
ENST00000441621.6:c.*519T>G	ENSP00000408819.2:n.*519T>G
ENST00000446616.1:c.*978T>G	ENSP00000410801.1:n.*978T>G
ENST00000543200.5:c.1292T>G	ENSP00000438380.1:p.Val431Gly
NM_000751.2:c.1337T>G	NP_000742.1:p.Val446Gly
NM_001256657.1:c.1292T>G	NP_001243586.1:p.Val431Gly
NM_001311195.1:c.755T>G	NP_001298124.1:p.Val252Gly
NM_001311196.1:c.1034T>G	NP_001298125.1:p.Val345Gly
NR_046333.1:c.-4294966214T>G
NR_046334.1:c.-4294965935T>G
XM_011510524.1:c.956T>G	XP_011508826.1:p.Val319Gly
XM_011510524.2:c.956T>G	XP_011508826.1:p.Val319Gly
NM_000751.3:c.1337T>G MANE Select	NP_000742.1:p.Val446Gly
NM_001311195.2:c.755T>G	NP_001298124.1:p.Val252Gly
NM_001311196.2:c.1034T>G	NP_001298125.1:p.Val345Gly
NM_001256657.2:c.1292T>G	NP_001243586.1:p.Val431Gly