Canonical Allele Identifier: CA351005305

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233398824G>C (hg19) ; chr2:g.232534114G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534114G>C , CM000664.2:g.232534114G>C	GRCh38
NC_000002.11:g.233398824G>C , CM000664.1:g.233398824G>C	GRCh37
NC_000002.10:g.233107068G>C	NCBI36
NG_008028.1:g.12903G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1231G>C MANE Select	ENSP00000258385.3:p.Ala411Pro
ENST00000258385.7:c.1231G>C	ENSP00000258385.3:p.Ala411Pro
ENST00000441621.6:c.*413G>C	ENSP00000408819.2:n.*413G>C
ENST00000446616.1:c.*872G>C	ENSP00000410801.1:n.*872G>C
ENST00000543200.5:c.1186G>C	ENSP00000438380.1:p.Ala396Pro
NM_000751.2:c.1231G>C	NP_000742.1:p.Ala411Pro
NM_001256657.1:c.1186G>C	NP_001243586.1:p.Ala396Pro
NM_001311195.1:c.649G>C	NP_001298124.1:p.Ala217Pro
NM_001311196.1:c.928G>C	NP_001298125.1:p.Ala310Pro
NR_046333.1:c.-4294966320G>C
NR_046334.1:c.-4294966041G>C
XM_011510524.1:c.850G>C	XP_011508826.1:p.Ala284Pro
XM_011510524.2:c.850G>C	XP_011508826.1:p.Ala284Pro
NM_000751.3:c.1231G>C MANE Select	NP_000742.1:p.Ala411Pro
NM_001311195.2:c.649G>C	NP_001298124.1:p.Ala217Pro
NM_001311196.2:c.928G>C	NP_001298125.1:p.Ala310Pro
NM_001256657.2:c.1186G>C	NP_001243586.1:p.Ala396Pro