Canonical Allele Identifier: CA343767715
Gene: DARS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173857598C>A , CM000663.2:g.173857598C>A GRCh38
NC_000001.10:g.173826736C>A , CM000663.1:g.173826736C>A GRCh37
NC_000001.9:g.172093359C>A NCBI36
NG_016138.1:g.37940C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000471476.2:c.*1410C>A ENSP00000497663.1:n.*1410C>A
ENST00000647645.1:c.1768C>A ENSP00000497450.1:p.His590Asn
ENST00000647730.1:c.*1521C>A ENSP00000497781.1:n.*1521C>A
ENST00000647788.1:c.*975C>A ENSP00000497769.1:n.*975C>A
ENST00000648271.1:c.*2297C>A ENSP00000497795.1:n.*2297C>A
ENST00000648807.1:c.1678C>A ENSP00000497472.1:p.His560Asn
ENST00000648960.1:c.1348C>A ENSP00000497091.1:p.His450Asn
ENST00000649067.1:c.*834C>A ENSP00000497052.1:n.*834C>A
ENST00000649689.2:c.1831C>A MANE Select ENSP00000497569.1:p.His611Asn
ENST00000361951.4:c.1831C>A ENSP00000355086.4:p.His611Asn
ENST00000471476.1:n.653C>A
NM_018122.4:c.1831C>A NP_060592.2:p.His611Asn
XM_006711427.2:c.1678C>A XP_006711490.1:p.His560Asn
NM_001365212.1:c.1678C>A NP_001352141.1:p.His560Asn
NM_018122.5:c.1831C>A MANE Select NP_060592.2:p.His611Asn