Canonical Allele Identifier: CA431952463

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233399007A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534297A>G , CM000664.2:g.232534297A>G	GRCh38
NC_000002.11:g.233399007A>G , CM000664.1:g.233399007A>G	GRCh37
NC_000002.10:g.233107251A>G	NCBI36
NG_008028.1:g.13086A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1326A>G MANE Select	ENSP00000258385.3:p.Ala442=
ENST00000258385.7:c.1326A>G	ENSP00000258385.3:p.Ala442=
ENST00000441621.6:c.*508A>G	ENSP00000408819.2:n.*508A>G
ENST00000446616.1:c.*967A>G	ENSP00000410801.1:n.*967A>G
ENST00000543200.5:c.1281A>G	ENSP00000438380.1:p.Ala427=
NM_000751.2:c.1326A>G	NP_000742.1:p.Ala442=
NM_001256657.1:c.1281A>G	NP_001243586.1:p.Ala427=
NM_001311195.1:c.744A>G	NP_001298124.1:p.Ala248=
NM_001311196.1:c.1023A>G	NP_001298125.1:p.Ala341=
NR_046333.1:c.-4294966225A>G
NR_046334.1:c.-4294965946A>G
XM_011510524.1:c.945A>G	XP_011508826.1:p.Ala315=
XM_011510524.2:c.945A>G	XP_011508826.1:p.Ala315=
NM_000751.3:c.1326A>G MANE Select	NP_000742.1:p.Ala442=
NM_001311195.2:c.744A>G	NP_001298124.1:p.Ala248=
NM_001311196.2:c.1023A>G	NP_001298125.1:p.Ala341=
NM_001256657.2:c.1281A>G	NP_001243586.1:p.Ala427=