Canonical Allele Identifier: CA1250162
Community Standard Title: NM_018122.5(DARS2):c.562C>T (p.Arg188Ter)
Gene: DARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173833445C>T , CM000663.2:g.173833445C>T GRCh38
NC_000001.10:g.173802583C>T , CM000663.1:g.173802583C>T GRCh37
NC_000001.9:g.172069206C>T NCBI36
NG_016138.1:g.13787C>T

Transcript Alleles

HGVS Amino-acid Change
NM_018122.5:c.562C>T MANE Select NP_060592.2:p.Arg188Ter
ENST00000649689.2:c.562C>T MANE Select ENSP00000497569.1:p.Arg188Ter
NM_001365212.1:c.562C>T NP_001352141.1:p.Arg188Ter
NM_001365213.1:c.562C>T NP_001352142.1:p.Arg188Ter
NM_001365213.2:c.562C>T NP_001352142.1:p.Arg188Ter
NM_018122.4:c.562C>T NP_060592.2:p.Arg188Ter
ENST00000361951.4:c.562C>T ENSP00000355086.4:p.Arg188Ter
ENST00000471476.2:c.*252C>T ENSP00000497663.1:n.*252C>T
ENST00000647645.1:c.562C>T ENSP00000497450.1:p.Arg188Ter
ENST00000647730.1:c.*252C>T ENSP00000497781.1:n.*252C>T
ENST00000647788.1:c.*252C>T ENSP00000497769.1:n.*252C>T
ENST00000648271.1:c.*252C>T ENSP00000497795.1:n.*252C>T
ENST00000648458.1:c.562C>T ENSP00000497874.1:p.Arg188Ter
ENST00000648807.1:c.562C>T ENSP00000497472.1:p.Arg188Ter
ENST00000648960.1:c.562C>T ENSP00000497091.1:p.Arg188Ter
ENST00000649067.1:c.562C>T ENSP00000497052.1:p.Arg188Ter
ENST00000649106.1:c.18C>T
ENST00000650297.1:n.945C>T
XM_006711427.2:c.562C>T XP_006711490.1:p.Arg188Ter
XM_011509711.1:c.562C>T XP_011508013.1:p.Arg188Ter