Canonical Allele Identifier: CA2649165111
Gene: DARS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173857452_173857467del , CM000663.2:g.173857452_173857467del GRCh38
NC_000001.10:g.173826590_173826605del , CM000663.1:g.173826590_173826605del GRCh37
NC_000001.9:g.172093213_172093228del NCBI36
NG_016138.1:g.37794_37809del

Transcript Alleles

HGVS Amino-acid Change
ENST00000471476.2:c.*1330-66_*1330-51del ENSP00000497663.1:n.*1330-66_*1330-51del
ENST00000647645.1:c.1688-66_1688-51del ENSP00000497450.1:n.1688-66_1688-51del
ENST00000647730.1:c.*1441-66_*1441-51del ENSP00000497781.1:n.*1441-66_*1441-51del
ENST00000647788.1:c.*895-66_*895-51del ENSP00000497769.1:n.*895-66_*895-51del
ENST00000648271.1:c.*2151_*2166del ENSP00000497795.1:n.*2151_*2166del
ENST00000648807.1:c.1598-66_1598-51del ENSP00000497472.1:n.1598-66_1598-51del
ENST00000648960.1:c.1268-66_1268-51del ENSP00000497091.1:n.1268-66_1268-51del
ENST00000649067.1:c.*688_*703del ENSP00000497052.1:n.*688_*703del
ENST00000649689.2:c.1751-66_1751-51del MANE Select ENSP00000497569.1:n.1751-66_1751-51del
ENST00000361951.4:c.1751-66_1751-51del ENSP00000355086.4:n.1751-66_1751-51del
ENST00000471476.1:n.573-66_573-51del
NM_018122.4:c.1751-66_1751-51del NP_060592.2:n.1751-66_1751-51del
XM_006711427.2:c.1598-66_1598-51del XP_006711490.1:n.1598-66_1598-51del
NM_001365212.1:c.1598-66_1598-51del NP_001352141.1:n.1598-66_1598-51del
NM_018122.5:c.1751-66_1751-51del MANE Select NP_060592.2:n.1751-66_1751-51del