Canonical Allele Identifier: CA2649165093
Gene: DARS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173857421_173857423del , CM000663.2:g.173857421_173857423del GRCh38
NC_000001.10:g.173826559_173826561del , CM000663.1:g.173826559_173826561del GRCh37
NC_000001.9:g.172093182_172093184del NCBI36
NG_016138.1:g.37763_37765del

Transcript Alleles

HGVS Amino-acid Change
ENST00000471476.2:c.*1330-97_*1330-95del ENSP00000497663.1:n.*1330-97_*1330-95del
ENST00000647645.1:c.1688-97_1688-95del ENSP00000497450.1:n.1688-97_1688-95del
ENST00000647730.1:c.*1441-97_*1441-95del ENSP00000497781.1:n.*1441-97_*1441-95del
ENST00000647788.1:c.*895-97_*895-95del ENSP00000497769.1:n.*895-97_*895-95del
ENST00000648271.1:c.*2120_*2122del ENSP00000497795.1:n.*2120_*2122del
ENST00000648807.1:c.1598-97_1598-95del ENSP00000497472.1:n.1598-97_1598-95del
ENST00000648960.1:c.1268-97_1268-95del ENSP00000497091.1:n.1268-97_1268-95del
ENST00000649067.1:c.*657_*659del ENSP00000497052.1:n.*657_*659del
ENST00000649689.2:c.1751-97_1751-95del MANE Select ENSP00000497569.1:n.1751-97_1751-95del
ENST00000361951.4:c.1751-97_1751-95del ENSP00000355086.4:n.1751-97_1751-95del
ENST00000471476.1:n.573-97_573-95del
NM_018122.4:c.1751-97_1751-95del NP_060592.2:n.1751-97_1751-95del
XM_006711427.2:c.1598-97_1598-95del XP_006711490.1:n.1598-97_1598-95del
NM_001365212.1:c.1598-97_1598-95del NP_001352141.1:n.1598-97_1598-95del
NM_018122.5:c.1751-97_1751-95del MANE Select NP_060592.2:n.1751-97_1751-95del