Canonical Allele Identifier: CA431952421

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233398977C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534267C>T , CM000664.2:g.232534267C>T	GRCh38
NC_000002.11:g.233398977C>T , CM000664.1:g.233398977C>T	GRCh37
NC_000002.10:g.233107221C>T	NCBI36
NG_008028.1:g.13056C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1296C>T MANE Select	ENSP00000258385.3:p.Phe432=
ENST00000258385.7:c.1296C>T	ENSP00000258385.3:p.Phe432=
ENST00000441621.6:c.*478C>T	ENSP00000408819.2:n.*478C>T
ENST00000446616.1:c.*937C>T	ENSP00000410801.1:n.*937C>T
ENST00000543200.5:c.1251C>T	ENSP00000438380.1:p.Phe417=
NM_000751.2:c.1296C>T	NP_000742.1:p.Phe432=
NM_001256657.1:c.1251C>T	NP_001243586.1:p.Phe417=
NM_001311195.1:c.714C>T	NP_001298124.1:p.Phe238=
NM_001311196.1:c.993C>T	NP_001298125.1:p.Phe331=
NR_046333.1:c.-4294966255C>T
NR_046334.1:c.-4294965976C>T
XM_011510524.1:c.915C>T	XP_011508826.1:p.Phe305=
XM_011510524.2:c.915C>T	XP_011508826.1:p.Phe305=
NM_000751.3:c.1296C>T MANE Select	NP_000742.1:p.Phe432=
NM_001311195.2:c.714C>T	NP_001298124.1:p.Phe238=
NM_001311196.2:c.993C>T	NP_001298125.1:p.Phe331=
NM_001256657.2:c.1251C>T	NP_001243586.1:p.Phe417=