Canonical Allele Identifier: CA351005256

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233398801A>T (hg19) ; chr2:g.232534091A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534091A>T , CM000664.2:g.232534091A>T	GRCh38
NC_000002.11:g.233398801A>T , CM000664.1:g.233398801A>T	GRCh37
NC_000002.10:g.233107045A>T	NCBI36
NG_008028.1:g.12880A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000258385.8:c.1208A>T MANE Select	ENSP00000258385.3:p.Lys403Met
ENST00000258385.7:c.1208A>T	ENSP00000258385.3:p.Lys403Met
ENST00000441621.6:c.*390A>T	ENSP00000408819.2:n.*390A>T
ENST00000446616.1:c.*849A>T	ENSP00000410801.1:n.*849A>T
ENST00000543200.5:c.1163A>T	ENSP00000438380.1:p.Lys388Met
NM_000751.2:c.1208A>T	NP_000742.1:p.Lys403Met
NM_001256657.1:c.1163A>T	NP_001243586.1:p.Lys388Met
NM_001311195.1:c.626A>T	NP_001298124.1:p.Lys209Met
NM_001311196.1:c.905A>T	NP_001298125.1:p.Lys302Met
NR_046333.1:c.-4294966343A>T
NR_046334.1:c.-4294966064A>T
XM_011510524.1:c.827A>T	XP_011508826.1:p.Lys276Met
XM_011510524.2:c.827A>T	XP_011508826.1:p.Lys276Met
NM_000751.3:c.1208A>T MANE Select	NP_000742.1:p.Lys403Met
NM_001311195.2:c.626A>T	NP_001298124.1:p.Lys209Met
NM_001311196.2:c.905A>T	NP_001298125.1:p.Lys302Met
NM_001256657.2:c.1163A>T	NP_001243586.1:p.Lys388Met