Canonical Allele Identifier: CA2649163863
Gene: DARS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173831418_173831422del , CM000663.2:g.173831418_173831422del GRCh38
NC_000001.10:g.173800556_173800560del , CM000663.1:g.173800556_173800560del GRCh37
NC_000001.9:g.172067179_172067183del NCBI36
NG_016138.1:g.11760_11764del

Transcript Alleles

HGVS Amino-acid Change
ENST00000471476.2:c.*87-117_*87-113del ENSP00000497663.1:n.*87-117_*87-113del
ENST00000647645.1:c.397-117_397-113del ENSP00000497450.1:n.397-117_397-113del
ENST00000647730.1:c.*87-117_*87-113del ENSP00000497781.1:n.*87-117_*87-113del
ENST00000647788.1:c.*87-117_*87-113del ENSP00000497769.1:n.*87-117_*87-113del
ENST00000648271.1:c.*87-117_*87-113del ENSP00000497795.1:n.*87-117_*87-113del
ENST00000648458.1:c.397-117_397-113del ENSP00000497874.1:n.397-117_397-113del
ENST00000648807.1:c.397-117_397-113del ENSP00000497472.1:n.397-117_397-113del
ENST00000648960.1:c.397-117_397-113del ENSP00000497091.1:n.397-117_397-113del
ENST00000649067.1:c.397-117_397-113del ENSP00000497052.1:n.397-117_397-113del
ENST00000649689.2:c.397-117_397-113del MANE Select ENSP00000497569.1:n.397-117_397-113del
ENST00000650297.1:n.780-117_780-113del
ENST00000361951.4:c.397-117_397-113del ENSP00000355086.4:n.397-117_397-113del
NM_018122.4:c.397-117_397-113del NP_060592.2:n.397-117_397-113del
XM_006711427.2:c.397-117_397-113del XP_006711490.1:n.397-117_397-113del
XM_011509711.1:c.397-117_397-113del XP_011508013.1:n.397-117_397-113del
NM_001365212.1:c.397-117_397-113del NP_001352141.1:n.397-117_397-113del
NM_001365213.1:c.397-117_397-113del NP_001352142.1:n.397-117_397-113del
NM_018122.5:c.397-117_397-113del MANE Select NP_060592.2:n.397-117_397-113del
NM_001365213.2:c.397-117_397-113del NP_001352142.1:n.397-117_397-113del