Canonical Allele Identifier: CA1207913149

Gene: DARS2

Linked Data

• dbSNP Id: rs1653892606

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857394_173857396dup , CM000663.2:g.173857394_173857396dup	GRCh38
NC_000001.10:g.173826532_173826534dup , CM000663.1:g.173826532_173826534dup	GRCh37
NC_000001.9:g.172093155_172093157dup	NCBI36
NG_016138.1:g.37736_37738dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471476.2:c.*1330-124_*1330-122dup	ENSP00000497663.1:n.*1330-124_*1330-122dup
ENST00000647645.1:c.1688-124_1688-122dup	ENSP00000497450.1:n.1688-124_1688-122dup
ENST00000647730.1:c.*1441-124_*1441-122dup	ENSP00000497781.1:n.*1441-124_*1441-122dup
ENST00000647788.1:c.*895-124_*895-122dup	ENSP00000497769.1:n.*895-124_*895-122dup
ENST00000648271.1:c.*2093_*2095dup	ENSP00000497795.1:n.*2093_*2095dup
ENST00000648807.1:c.1598-124_1598-122dup	ENSP00000497472.1:n.1598-124_1598-122dup
ENST00000648960.1:c.1268-124_1268-122dup	ENSP00000497091.1:n.1268-124_1268-122dup
ENST00000649067.1:c.*630_*632dup	ENSP00000497052.1:n.*630_*632dup
ENST00000649689.2:c.1751-124_1751-122dup MANE Select	ENSP00000497569.1:n.1751-124_1751-122dup
ENST00000361951.4:c.1751-124_1751-122dup	ENSP00000355086.4:n.1751-124_1751-122dup
ENST00000471476.1:n.573-124_573-122dup
NM_018122.4:c.1751-124_1751-122dup	NP_060592.2:n.1751-124_1751-122dup
XM_006711427.2:c.1598-124_1598-122dup	XP_006711490.1:n.1598-124_1598-122dup
NM_001365212.1:c.1598-124_1598-122dup	NP_001352141.1:n.1598-124_1598-122dup
NM_018122.5:c.1751-124_1751-122dup MANE Select	NP_060592.2:n.1751-124_1751-122dup