Canonical Allele Identifier: CA891309326

Gene: DARS2

Linked Data

• dbSNP Id: rs1273214140
• MyVariant Identifiers: chr1:g.173826434_173826441del (hg19) ; chr1:g.173857296_173857303del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857297_173857304del , CM000663.2:g.173857297_173857304del	GRCh38
NC_000001.10:g.173826435_173826442del , CM000663.1:g.173826435_173826442del	GRCh37
NC_000001.9:g.172093058_172093065del	NCBI36
NG_016138.1:g.37639_37646del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471476.2:c.*1330-221_*1330-214del	ENSP00000497663.1:n.*1330-221_*1330-214del
ENST00000647645.1:c.1688-221_1688-214del	ENSP00000497450.1:n.1688-221_1688-214del
ENST00000647730.1:c.*1441-221_*1441-214del	ENSP00000497781.1:n.*1441-221_*1441-214del
ENST00000647788.1:c.*895-221_*895-214del	ENSP00000497769.1:n.*895-221_*895-214del
ENST00000648271.1:c.*1996_*2003del	ENSP00000497795.1:n.*1996_*2003del
ENST00000648807.1:c.1598-221_1598-214del	ENSP00000497472.1:n.1598-221_1598-214del
ENST00000648960.1:c.1268-221_1268-214del	ENSP00000497091.1:n.1268-221_1268-214del
ENST00000649067.1:c.*533_*540del	ENSP00000497052.1:n.*533_*540del
ENST00000649689.2:c.1751-221_1751-214del MANE Select	ENSP00000497569.1:n.1751-221_1751-214del
ENST00000361951.4:c.1751-221_1751-214del	ENSP00000355086.4:n.1751-221_1751-214del
ENST00000471476.1:n.573-221_573-214del
NM_018122.4:c.1751-221_1751-214del	NP_060592.2:n.1751-221_1751-214del
XM_006711427.2:c.1598-221_1598-214del	XP_006711490.1:n.1598-221_1598-214del
NM_001365212.1:c.1598-221_1598-214del	NP_001352141.1:n.1598-221_1598-214del
NM_018122.5:c.1751-221_1751-214del MANE Select	NP_060592.2:n.1751-221_1751-214del