Canonical Allele Identifier: CA351005671

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233398997T>G (hg19) ; chr2:g.232534287T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534287T>G , CM000664.2:g.232534287T>G	GRCh38
NC_000002.11:g.233398997T>G , CM000664.1:g.233398997T>G	GRCh37
NC_000002.10:g.233107241T>G	NCBI36
NG_008028.1:g.13076T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1316T>G MANE Select	ENSP00000258385.3:p.Val439Gly
ENST00000258385.7:c.1316T>G	ENSP00000258385.3:p.Val439Gly
ENST00000441621.6:c.*498T>G	ENSP00000408819.2:n.*498T>G
ENST00000446616.1:c.*957T>G	ENSP00000410801.1:n.*957T>G
ENST00000543200.5:c.1271T>G	ENSP00000438380.1:p.Val424Gly
NM_000751.2:c.1316T>G	NP_000742.1:p.Val439Gly
NM_001256657.1:c.1271T>G	NP_001243586.1:p.Val424Gly
NM_001311195.1:c.734T>G	NP_001298124.1:p.Val245Gly
NM_001311196.1:c.1013T>G	NP_001298125.1:p.Val338Gly
NR_046333.1:c.-4294966235T>G
NR_046334.1:c.-4294965956T>G
XM_011510524.1:c.935T>G	XP_011508826.1:p.Val312Gly
XM_011510524.2:c.935T>G	XP_011508826.1:p.Val312Gly
NM_000751.3:c.1316T>G MANE Select	NP_000742.1:p.Val439Gly
NM_001311195.2:c.734T>G	NP_001298124.1:p.Val245Gly
NM_001311196.2:c.1013T>G	NP_001298125.1:p.Val338Gly
NM_001256657.2:c.1271T>G	NP_001243586.1:p.Val424Gly