Canonical Allele Identifier: CA431952578

Gene: CHRND

Linked Data

• dbSNP Id: rs1691806503
• MyVariant Identifiers: chr2:g.233398829G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534119G>A , CM000664.2:g.232534119G>A	GRCh38
NC_000002.11:g.233398829G>A , CM000664.1:g.233398829G>A	GRCh37
NC_000002.10:g.233107073G>A	NCBI36
NG_008028.1:g.12908G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1236G>A MANE Select	ENSP00000258385.3:p.Arg412=
ENST00000258385.7:c.1236G>A	ENSP00000258385.3:p.Arg412=
ENST00000441621.6:c.*418G>A	ENSP00000408819.2:n.*418G>A
ENST00000446616.1:c.*877G>A	ENSP00000410801.1:n.*877G>A
ENST00000543200.5:c.1191G>A	ENSP00000438380.1:p.Arg397=
NM_000751.2:c.1236G>A	NP_000742.1:p.Arg412=
NM_001256657.1:c.1191G>A	NP_001243586.1:p.Arg397=
NM_001311195.1:c.654G>A	NP_001298124.1:p.Arg218=
NM_001311196.1:c.933G>A	NP_001298125.1:p.Arg311=
NR_046333.1:c.-4294966315G>A
NR_046334.1:c.-4294966036G>A
XM_011510524.1:c.855G>A	XP_011508826.1:p.Arg285=
XM_011510524.2:c.855G>A	XP_011508826.1:p.Arg285=
NM_000751.3:c.1236G>A MANE Select	NP_000742.1:p.Arg412=
NM_001311195.2:c.654G>A	NP_001298124.1:p.Arg218=
NM_001311196.2:c.933G>A	NP_001298125.1:p.Arg311=
NM_001256657.2:c.1191G>A	NP_001243586.1:p.Arg397=