Canonical Allele Identifier: CA1207913139
Gene: DARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173857362_173857367delinsCAAACA , CM000663.2:g.173857362_173857367delinsCAAACA GRCh38
NC_000001.10:g.173826500_173826505delinsCAAACA , CM000663.1:g.173826500_173826505delinsCAAACA GRCh37
NC_000001.9:g.172093123_172093128delinsCAAACA NCBI36
NG_016138.1:g.37704_37709delinsCAAACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000471476.2:c.*1330-156_*1330-151delinsCAAACA ENSP00000497663.1:n.*1330-156_*1330-151delinsCAAACA
ENST00000647645.1:c.1688-156_1688-151delinsCAAACA ENSP00000497450.1:n.1688-156_1688-151delinsCAAACA
ENST00000647730.1:c.*1441-156_*1441-151delinsCAAACA ENSP00000497781.1:n.*1441-156_*1441-151delinsCAAACA
ENST00000647788.1:c.*895-156_*895-151delinsCAAACA ENSP00000497769.1:n.*895-156_*895-151delinsCAAACA
ENST00000648271.1:c.*2061_*2066delinsCAAACA ENSP00000497795.1:n.*2061_*2066delinsCAAACA
ENST00000648807.1:c.1598-156_1598-151delinsCAAACA ENSP00000497472.1:n.1598-156_1598-151delinsCAAACA
ENST00000648960.1:c.1268-156_1268-151delinsCAAACA ENSP00000497091.1:n.1268-156_1268-151delinsCAAACA
ENST00000649067.1:c.*598_*603delinsCAAACA ENSP00000497052.1:n.*598_*603delinsCAAACA
ENST00000649689.2:c.1751-156_1751-151delinsCAAACA MANE Select ENSP00000497569.1:n.1751-156_1751-151delinsCAAACA
ENST00000361951.4:c.1751-156_1751-151delinsCAAACA ENSP00000355086.4:n.1751-156_1751-151delinsCAAACA
ENST00000471476.1:n.573-156_573-151delinsCAAACA
NM_018122.4:c.1751-156_1751-151delinsCAAACA NP_060592.2:n.1751-156_1751-151delinsCAAACA
XM_006711427.2:c.1598-156_1598-151delinsCAAACA XP_006711490.1:n.1598-156_1598-151delinsCAAACA
NM_001365212.1:c.1598-156_1598-151delinsCAAACA NP_001352141.1:n.1598-156_1598-151delinsCAAACA
NM_018122.5:c.1751-156_1751-151delinsCAAACA MANE Select NP_060592.2:n.1751-156_1751-151delinsCAAACA