Canonical Allele Identifier: CA2649165094
Gene: DARS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173857419_173857427del , CM000663.2:g.173857419_173857427del GRCh38
NC_000001.10:g.173826557_173826565del , CM000663.1:g.173826557_173826565del GRCh37
NC_000001.9:g.172093180_172093188del NCBI36
NG_016138.1:g.37761_37769del

Transcript Alleles

HGVS Amino-acid Change
ENST00000471476.2:c.*1330-99_*1330-91del ENSP00000497663.1:n.*1330-99_*1330-91del
ENST00000647645.1:c.1688-99_1688-91del ENSP00000497450.1:n.1688-99_1688-91del
ENST00000647730.1:c.*1441-99_*1441-91del ENSP00000497781.1:n.*1441-99_*1441-91del
ENST00000647788.1:c.*895-99_*895-91del ENSP00000497769.1:n.*895-99_*895-91del
ENST00000648271.1:c.*2118_*2126del ENSP00000497795.1:n.*2118_*2126del
ENST00000648807.1:c.1598-99_1598-91del ENSP00000497472.1:n.1598-99_1598-91del
ENST00000648960.1:c.1268-99_1268-91del ENSP00000497091.1:n.1268-99_1268-91del
ENST00000649067.1:c.*655_*663del ENSP00000497052.1:n.*655_*663del
ENST00000649689.2:c.1751-99_1751-91del MANE Select ENSP00000497569.1:n.1751-99_1751-91del
ENST00000361951.4:c.1751-99_1751-91del ENSP00000355086.4:n.1751-99_1751-91del
ENST00000471476.1:n.573-99_573-91del
NM_018122.4:c.1751-99_1751-91del NP_060592.2:n.1751-99_1751-91del
XM_006711427.2:c.1598-99_1598-91del XP_006711490.1:n.1598-99_1598-91del
NM_001365212.1:c.1598-99_1598-91del NP_001352141.1:n.1598-99_1598-91del
NM_018122.5:c.1751-99_1751-91del MANE Select NP_060592.2:n.1751-99_1751-91del