Canonical Allele Identifier: CA351005804

Gene: CHRND

Linked Data

• MyVariant Identifiers: chr2:g.233399027T>G (hg19) ; chr2:g.232534317T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232534317T>G , CM000664.2:g.232534317T>G	GRCh38
NC_000002.11:g.233399027T>G , CM000664.1:g.233399027T>G	GRCh37
NC_000002.10:g.233107271T>G	NCBI36
NG_008028.1:g.13106T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258385.8:c.1346T>G MANE Select	ENSP00000258385.3:p.Met449Arg
ENST00000258385.7:c.1346T>G	ENSP00000258385.3:p.Met449Arg
ENST00000441621.6:c.*528T>G	ENSP00000408819.2:n.*528T>G
ENST00000446616.1:c.*987T>G	ENSP00000410801.1:n.*987T>G
ENST00000543200.5:c.1301T>G	ENSP00000438380.1:p.Met434Arg
NM_000751.2:c.1346T>G	NP_000742.1:p.Met449Arg
NM_001256657.1:c.1301T>G	NP_001243586.1:p.Met434Arg
NM_001311195.1:c.764T>G	NP_001298124.1:p.Met255Arg
NM_001311196.1:c.1043T>G	NP_001298125.1:p.Met348Arg
NR_046333.1:c.-4294966205T>G
NR_046334.1:c.-4294965926T>G
XM_011510524.1:c.965T>G	XP_011508826.1:p.Met322Arg
XM_011510524.2:c.965T>G	XP_011508826.1:p.Met322Arg
NM_000751.3:c.1346T>G MANE Select	NP_000742.1:p.Met449Arg
NM_001311195.2:c.764T>G	NP_001298124.1:p.Met255Arg
NM_001311196.2:c.1043T>G	NP_001298125.1:p.Met348Arg
NM_001256657.2:c.1301T>G	NP_001243586.1:p.Met434Arg