Canonical Allele Identifier: CA431952427

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233398984C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534274C>T , CM000664.2:g.232534274C>T	GRCh38
NC_000002.11:g.233398984C>T , CM000664.1:g.233398984C>T	GRCh37
NC_000002.10:g.233107228C>T	NCBI36
NG_008028.1:g.13063C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1303C>T MANE Select	ENSP00000258385.3:p.Leu435=
ENST00000258385.7:c.1303C>T	ENSP00000258385.3:p.Leu435=
ENST00000441621.6:c.*485C>T	ENSP00000408819.2:n.*485C>T
ENST00000446616.1:c.*944C>T	ENSP00000410801.1:n.*944C>T
ENST00000543200.5:c.1258C>T	ENSP00000438380.1:p.Leu420=
NM_000751.2:c.1303C>T	NP_000742.1:p.Leu435=
NM_001256657.1:c.1258C>T	NP_001243586.1:p.Leu420=
NM_001311195.1:c.721C>T	NP_001298124.1:p.Leu241=
NM_001311196.1:c.1000C>T	NP_001298125.1:p.Leu334=
NR_046333.1:c.-4294966248C>T
NR_046334.1:c.-4294965969C>T
XM_011510524.1:c.922C>T	XP_011508826.1:p.Leu308=
XM_011510524.2:c.922C>T	XP_011508826.1:p.Leu308=
NM_000751.3:c.1303C>T MANE Select	NP_000742.1:p.Leu435=
NM_001311195.2:c.721C>T	NP_001298124.1:p.Leu241=
NM_001311196.2:c.1000C>T	NP_001298125.1:p.Leu334=
NM_001256657.2:c.1258C>T	NP_001243586.1:p.Leu420=