Canonical Allele Identifier: CA351005186

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233398768T>C (hg19) ; chr2:g.232534058T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534058T>C , CM000664.2:g.232534058T>C	GRCh38
NC_000002.11:g.233398768T>C , CM000664.1:g.233398768T>C	GRCh37
NC_000002.10:g.233107012T>C	NCBI36
NG_008028.1:g.12847T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1175T>C MANE Select	ENSP00000258385.3:p.Leu392Pro
ENST00000258385.7:c.1175T>C	ENSP00000258385.3:p.Leu392Pro
ENST00000441621.6:c.*357T>C	ENSP00000408819.2:n.*357T>C
ENST00000446616.1:c.*816T>C	ENSP00000410801.1:n.*816T>C
ENST00000543200.5:c.1130T>C	ENSP00000438380.1:p.Leu377Pro
NM_000751.2:c.1175T>C	NP_000742.1:p.Leu392Pro
NM_001256657.1:c.1130T>C	NP_001243586.1:p.Leu377Pro
NM_001311195.1:c.593T>C	NP_001298124.1:p.Leu198Pro
NM_001311196.1:c.872T>C	NP_001298125.1:p.Leu291Pro
NR_046333.1:c.-4294966376T>C
NR_046334.1:c.-4294966097T>C
XM_011510524.1:c.794T>C	XP_011508826.1:p.Leu265Pro
XM_011510524.2:c.794T>C	XP_011508826.1:p.Leu265Pro
NM_000751.3:c.1175T>C MANE Select	NP_000742.1:p.Leu392Pro
NM_001311195.2:c.593T>C	NP_001298124.1:p.Leu198Pro
NM_001311196.2:c.872T>C	NP_001298125.1:p.Leu291Pro
NM_001256657.2:c.1130T>C	NP_001243586.1:p.Leu377Pro