Canonical Allele Identifier: CA1207913120
Gene: DARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173857318_173857319delinsTC , CM000663.2:g.173857318_173857319delinsTC GRCh38
NC_000001.10:g.173826456_173826457delinsTC , CM000663.1:g.173826456_173826457delinsTC GRCh37
NC_000001.9:g.172093079_172093080delinsTC NCBI36
NG_016138.1:g.37660_37661delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000471476.2:c.*1330-200_*1330-199delinsTC ENSP00000497663.1:n.*1330-200_*1330-199delinsTC
ENST00000647645.1:c.1688-200_1688-199delinsTC ENSP00000497450.1:n.1688-200_1688-199delinsTC
ENST00000647730.1:c.*1441-200_*1441-199delinsTC ENSP00000497781.1:n.*1441-200_*1441-199delinsTC
ENST00000647788.1:c.*895-200_*895-199delinsTC ENSP00000497769.1:n.*895-200_*895-199delinsTC
ENST00000648271.1:c.*2017_*2018delinsTC ENSP00000497795.1:n.*2017_*2018delinsTC
ENST00000648807.1:c.1598-200_1598-199delinsTC ENSP00000497472.1:n.1598-200_1598-199delinsTC
ENST00000648960.1:c.1268-200_1268-199delinsTC ENSP00000497091.1:n.1268-200_1268-199delinsTC
ENST00000649067.1:c.*554_*555delinsTC ENSP00000497052.1:n.*554_*555delinsTC
ENST00000649689.2:c.1751-200_1751-199delinsTC MANE Select ENSP00000497569.1:n.1751-200_1751-199delinsTC
ENST00000361951.4:c.1751-200_1751-199delinsTC ENSP00000355086.4:n.1751-200_1751-199delinsTC
ENST00000471476.1:n.573-200_573-199delinsTC
NM_018122.4:c.1751-200_1751-199delinsTC NP_060592.2:n.1751-200_1751-199delinsTC
XM_006711427.2:c.1598-200_1598-199delinsTC XP_006711490.1:n.1598-200_1598-199delinsTC
NM_001365212.1:c.1598-200_1598-199delinsTC NP_001352141.1:n.1598-200_1598-199delinsTC
NM_018122.5:c.1751-200_1751-199delinsTC MANE Select NP_060592.2:n.1751-200_1751-199delinsTC