Canonical Allele Identifier: CA2649165087
Gene: DARS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173857409_173857410del , CM000663.2:g.173857409_173857410del GRCh38
NC_000001.10:g.173826547_173826548del , CM000663.1:g.173826547_173826548del GRCh37
NC_000001.9:g.172093170_172093171del NCBI36
NG_016138.1:g.37751_37752del

Transcript Alleles

HGVS Amino-acid Change
ENST00000471476.2:c.*1330-109_*1330-108del ENSP00000497663.1:n.*1330-109_*1330-108del
ENST00000647645.1:c.1688-109_1688-108del ENSP00000497450.1:n.1688-109_1688-108del
ENST00000647730.1:c.*1441-109_*1441-108del ENSP00000497781.1:n.*1441-109_*1441-108del
ENST00000647788.1:c.*895-109_*895-108del ENSP00000497769.1:n.*895-109_*895-108del
ENST00000648271.1:c.*2108_*2109del ENSP00000497795.1:n.*2108_*2109del
ENST00000648807.1:c.1598-109_1598-108del ENSP00000497472.1:n.1598-109_1598-108del
ENST00000648960.1:c.1268-109_1268-108del ENSP00000497091.1:n.1268-109_1268-108del
ENST00000649067.1:c.*645_*646del ENSP00000497052.1:n.*645_*646del
ENST00000649689.2:c.1751-109_1751-108del MANE Select ENSP00000497569.1:n.1751-109_1751-108del
ENST00000361951.4:c.1751-109_1751-108del ENSP00000355086.4:n.1751-109_1751-108del
ENST00000471476.1:n.573-109_573-108del
NM_018122.4:c.1751-109_1751-108del NP_060592.2:n.1751-109_1751-108del
XM_006711427.2:c.1598-109_1598-108del XP_006711490.1:n.1598-109_1598-108del
NM_001365212.1:c.1598-109_1598-108del NP_001352141.1:n.1598-109_1598-108del
NM_018122.5:c.1751-109_1751-108del MANE Select NP_060592.2:n.1751-109_1751-108del