Canonical Allele Identifier: CA2649163900

Gene: DARS2

Linked Data

• gnomAD v4: 1-173831512-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173831515del , CM000663.2:g.173831515del	GRCh38
NC_000001.10:g.173800653del , CM000663.1:g.173800653del	GRCh37
NC_000001.9:g.172067276del	NCBI36
NG_016138.1:g.11857del

Transcript Alleles

HGVS	Amino-acid change
ENST00000471476.2:c.*87-20del	ENSP00000497663.1:n.*87-20del
ENST00000647645.1:c.397-20del	ENSP00000497450.1:n.397-20del
ENST00000647730.1:c.*87-20del	ENSP00000497781.1:n.*87-20del
ENST00000647788.1:c.*87-20del	ENSP00000497769.1:n.*87-20del
ENST00000648271.1:c.*87-20del	ENSP00000497795.1:n.*87-20del
ENST00000648458.1:c.397-20del	ENSP00000497874.1:n.397-20del
ENST00000648807.1:c.397-20del	ENSP00000497472.1:n.397-20del
ENST00000648960.1:c.397-20del	ENSP00000497091.1:n.397-20del
ENST00000649067.1:c.397-20del	ENSP00000497052.1:n.397-20del
ENST00000649689.2:c.397-20del MANE Select	ENSP00000497569.1:n.397-20del
ENST00000650297.1:n.780-20del
ENST00000361951.4:c.397-20del	ENSP00000355086.4:n.397-20del
NM_018122.4:c.397-20del	NP_060592.2:n.397-20del
XM_006711427.2:c.397-20del	XP_006711490.1:n.397-20del
XM_011509711.1:c.397-20del	XP_011508013.1:n.397-20del
NM_001365212.1:c.397-20del	NP_001352141.1:n.397-20del
NM_001365213.1:c.397-20del	NP_001352142.1:n.397-20del
NM_018122.5:c.397-20del MANE Select	NP_060592.2:n.397-20del
NM_001365213.2:c.397-20del	NP_001352142.1:n.397-20del