Canonical Allele Identifier: CA343767745

Gene: DARS2

Linked Data

• MyVariant Identifiers: chr1:g.173826748A>C (hg19) ; chr1:g.173857610A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857610A>C , CM000663.2:g.173857610A>C	GRCh38
NC_000001.10:g.173826748A>C , CM000663.1:g.173826748A>C	GRCh37
NC_000001.9:g.172093371A>C	NCBI36
NG_016138.1:g.37952A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471476.2:c.*1422A>C	ENSP00000497663.1:n.*1422A>C
ENST00000647645.1:c.1780A>C	ENSP00000497450.1:p.Ser594Arg
ENST00000647730.1:c.*1533A>C	ENSP00000497781.1:n.*1533A>C
ENST00000647788.1:c.*987A>C	ENSP00000497769.1:n.*987A>C
ENST00000648271.1:c.*2309A>C	ENSP00000497795.1:n.*2309A>C
ENST00000648807.1:c.1690A>C	ENSP00000497472.1:p.Ser564Arg
ENST00000648960.1:c.1360A>C	ENSP00000497091.1:p.Ser454Arg
ENST00000649067.1:c.*846A>C	ENSP00000497052.1:n.*846A>C
ENST00000649689.2:c.1843A>C MANE Select	ENSP00000497569.1:p.Ser615Arg
ENST00000361951.4:c.1843A>C	ENSP00000355086.4:p.Ser615Arg
ENST00000471476.1:n.665A>C
NM_018122.4:c.1843A>C	NP_060592.2:p.Ser615Arg
XM_006711427.2:c.1690A>C	XP_006711490.1:p.Ser564Arg
NM_001365212.1:c.1690A>C	NP_001352141.1:p.Ser564Arg
NM_018122.5:c.1843A>C MANE Select	NP_060592.2:p.Ser615Arg