Canonical Allele Identifier: CA351005648

Gene: CHRND

Linked Data

• dbSNP Id: rs1360012669
• gnomAD v2: 2-233398991-C-G
• gnomAD v3: 2-232534281-C-G
• gnomAD v4: 2-232534281-C-G
• MyVariant Identifiers: chr2:g.233398991C>G (hg19) ; chr2:g.232534281C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534281C>G , CM000664.2:g.232534281C>G	GRCh38
NC_000002.11:g.233398991C>G , CM000664.1:g.233398991C>G	GRCh37
NC_000002.10:g.233107235C>G	NCBI36
NG_008028.1:g.13070C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1310C>G MANE Select	ENSP00000258385.3:p.Pro437Arg
ENST00000258385.7:c.1310C>G	ENSP00000258385.3:p.Pro437Arg
ENST00000441621.6:c.*492C>G	ENSP00000408819.2:n.*492C>G
ENST00000446616.1:c.*951C>G	ENSP00000410801.1:n.*951C>G
ENST00000543200.5:c.1265C>G	ENSP00000438380.1:p.Pro422Arg
NM_000751.2:c.1310C>G	NP_000742.1:p.Pro437Arg
NM_001256657.1:c.1265C>G	NP_001243586.1:p.Pro422Arg
NM_001311195.1:c.728C>G	NP_001298124.1:p.Pro243Arg
NM_001311196.1:c.1007C>G	NP_001298125.1:p.Pro336Arg
NR_046333.1:c.-4294966241C>G
NR_046334.1:c.-4294965962C>G
XM_011510524.1:c.929C>G	XP_011508826.1:p.Pro310Arg
XM_011510524.2:c.929C>G	XP_011508826.1:p.Pro310Arg
NM_000751.3:c.1310C>G MANE Select	NP_000742.1:p.Pro437Arg
NM_001311195.2:c.728C>G	NP_001298124.1:p.Pro243Arg
NM_001311196.2:c.1007C>G	NP_001298125.1:p.Pro336Arg
NM_001256657.2:c.1265C>G	NP_001243586.1:p.Pro422Arg