Canonical Allele Identifier: CA2168320

Gene: CHRND

Linked Data

• ClinVar Variation Id: 2164221
• ClinVar RCV Id: RCV003082044
• dbSNP Id: rs377734777
• ExAC: 2:233398979 A / G
• gnomAD v2: 2-233398979-A-G
• gnomAD v3: 2-232534269-A-G
• gnomAD v4: 2-232534269-A-G
• MyVariant Identifiers: chr2:g.233398979A>G (hg19) ; chr2:g.232534269A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534269A>G , CM000664.2:g.232534269A>G	GRCh38
NC_000002.11:g.233398979A>G , CM000664.1:g.233398979A>G	GRCh37
NC_000002.10:g.233107223A>G	NCBI36
NG_008028.1:g.13058A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1298A>G MANE Select	ENSP00000258385.3:p.Asn433Ser
ENST00000258385.7:c.1298A>G	ENSP00000258385.3:p.Asn433Ser
ENST00000441621.6:c.*480A>G	ENSP00000408819.2:n.*480A>G
ENST00000446616.1:c.*939A>G	ENSP00000410801.1:n.*939A>G
ENST00000543200.5:c.1253A>G	ENSP00000438380.1:p.Asn418Ser
NM_000751.2:c.1298A>G	NP_000742.1:p.Asn433Ser
NM_001256657.1:c.1253A>G	NP_001243586.1:p.Asn418Ser
NM_001311195.1:c.716A>G	NP_001298124.1:p.Asn239Ser
NM_001311196.1:c.995A>G	NP_001298125.1:p.Asn332Ser
NR_046333.1:c.-4294966253A>G
NR_046334.1:c.-4294965974A>G
XM_011510524.1:c.917A>G	XP_011508826.1:p.Asn306Ser
XM_011510524.2:c.917A>G	XP_011508826.1:p.Asn306Ser
NM_000751.3:c.1298A>G MANE Select	NP_000742.1:p.Asn433Ser
NM_001311195.2:c.716A>G	NP_001298124.1:p.Asn239Ser
NM_001311196.2:c.995A>G	NP_001298125.1:p.Asn332Ser
NM_001256657.2:c.1253A>G	NP_001243586.1:p.Asn418Ser