Canonical Allele Identifier: CA351005234

Gene: CHRND

Linked Data

• dbSNP Id: rs1366312082
• gnomAD v3: 2-232534081-A-G
• gnomAD v4: 2-232534081-A-G
• MyVariant Identifiers: chr2:g.233398791A>G (hg19) ; chr2:g.232534081A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534081A>G , CM000664.2:g.232534081A>G	GRCh38
NC_000002.11:g.233398791A>G , CM000664.1:g.233398791A>G	GRCh37
NC_000002.10:g.233107035A>G	NCBI36
NG_008028.1:g.12870A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1198A>G MANE Select	ENSP00000258385.3:p.Met400Val
ENST00000258385.7:c.1198A>G	ENSP00000258385.3:p.Met400Val
ENST00000441621.6:c.*380A>G	ENSP00000408819.2:n.*380A>G
ENST00000446616.1:c.*839A>G	ENSP00000410801.1:n.*839A>G
ENST00000543200.5:c.1153A>G	ENSP00000438380.1:p.Met385Val
NM_000751.2:c.1198A>G	NP_000742.1:p.Met400Val
NM_001256657.1:c.1153A>G	NP_001243586.1:p.Met385Val
NM_001311195.1:c.616A>G	NP_001298124.1:p.Met206Val
NM_001311196.1:c.895A>G	NP_001298125.1:p.Met299Val
NR_046333.1:c.-4294966353A>G
NR_046334.1:c.-4294966074A>G
XM_011510524.1:c.817A>G	XP_011508826.1:p.Met273Val
XM_011510524.2:c.817A>G	XP_011508826.1:p.Met273Val
NM_000751.3:c.1198A>G MANE Select	NP_000742.1:p.Met400Val
NM_001311195.2:c.616A>G	NP_001298124.1:p.Met206Val
NM_001311196.2:c.895A>G	NP_001298125.1:p.Met299Val
NM_001256657.2:c.1153A>G	NP_001243586.1:p.Met385Val