Canonical Allele Identifier: CA431952095

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233393031G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232528321G>A , CM000664.2:g.232528321G>A	GRCh38
NC_000002.11:g.233393031G>A , CM000664.1:g.233393031G>A	GRCh37
NC_000002.10:g.233101275G>A	NCBI36
NG_008028.1:g.7110G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.303G>A MANE Select	ENSP00000258385.3:p.Leu101=
ENST00000258385.7:c.303G>A	ENSP00000258385.3:p.Leu101=
ENST00000412233.5:c.303G>A	ENSP00000398143.1:p.Leu101=
ENST00000441621.6:c.303G>A	ENSP00000408819.2:p.Leu101=
ENST00000446616.1:c.303G>A	ENSP00000410801.1:p.Leu101=
ENST00000449596.5:c.258G>A	ENSP00000404950.1:p.Leu86=
ENST00000543200.5:c.258G>A	ENSP00000438380.1:p.Leu86=
NM_000751.2:c.303G>A	NP_000742.1:p.Leu101=
NM_001256657.1:c.258G>A	NP_001243586.1:p.Leu86=
NM_001311195.1:c.32G>A	NP_001298124.1:p.Cys11Tyr
NM_001311196.1:c.32G>A	NP_001298125.1:p.Cys11Tyr
NR_046333.1:c.-4294966937G>A
NR_046334.1:c.-4294966937G>A
XM_011510524.1:c.32G>A	XP_011508826.1:p.Cys11Tyr
XM_011510524.2:c.32G>A	XP_011508826.1:p.Cys11Tyr
NM_000751.3:c.303G>A MANE Select	NP_000742.1:p.Leu101=
NM_001311195.2:c.32G>A	NP_001298124.1:p.Cys11Tyr
NM_001311196.2:c.32G>A	NP_001298125.1:p.Cys11Tyr
NM_001256657.2:c.258G>A	NP_001243586.1:p.Leu86=