Canonical Allele Identifier: CA350997389

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233392978A>T (hg19) ; chr2:g.232528268A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232528268A>T , CM000664.2:g.232528268A>T	GRCh38
NC_000002.11:g.233392978A>T , CM000664.1:g.233392978A>T	GRCh37
NC_000002.10:g.233101222A>T	NCBI36
NG_008028.1:g.7057A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.250A>T MANE Select	ENSP00000258385.3:p.Thr84Ser
ENST00000258385.7:c.250A>T	ENSP00000258385.3:p.Thr84Ser
ENST00000412233.5:c.250A>T	ENSP00000398143.1:p.Thr84Ser
ENST00000441621.6:c.250A>T	ENSP00000408819.2:p.Thr84Ser
ENST00000446616.1:c.250A>T	ENSP00000410801.1:p.Thr84Ser
ENST00000449596.5:c.205A>T	ENSP00000404950.1:p.Thr69Ser
ENST00000543200.5:c.205A>T	ENSP00000438380.1:p.Thr69Ser
NM_000751.2:c.250A>T	NP_000742.1:p.Thr84Ser
NM_001256657.1:c.205A>T	NP_001243586.1:p.Thr69Ser
NM_001311195.1:c.-22A>T	NP_001298124.1:n.-22A>T
NM_001311196.1:c.-22A>T	NP_001298125.1:n.-22A>T
NR_046333.1:c.-4294966990A>T
NR_046334.1:c.-4294966990A>T
XM_011510524.1:c.-22A>T	XP_011508826.1:n.-22A>T
XM_011510524.2:c.-22A>T	XP_011508826.1:n.-22A>T
NM_000751.3:c.250A>T MANE Select	NP_000742.1:p.Thr84Ser
NM_001311195.2:c.-22A>T	NP_001298124.1:n.-22A>T
NM_001311196.2:c.-22A>T	NP_001298125.1:n.-22A>T
NM_001256657.2:c.205A>T	NP_001243586.1:p.Thr69Ser