Canonical Allele Identifier: CA421811966

Gene: DARS2

Linked Data

• gnomAD v4: 1-173857594-G-A
• MyVariant Identifiers: chr1:g.173826732G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857594G>A , CM000663.2:g.173857594G>A	GRCh38
NC_000001.10:g.173826732G>A , CM000663.1:g.173826732G>A	GRCh37
NC_000001.9:g.172093355G>A	NCBI36
NG_016138.1:g.37936G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000471476.2:c.*1406G>A	ENSP00000497663.1:n.*1406G>A
ENST00000647645.1:c.1764G>A	ENSP00000497450.1:p.Arg588=
ENST00000647730.1:c.*1517G>A	ENSP00000497781.1:n.*1517G>A
ENST00000647788.1:c.*971G>A	ENSP00000497769.1:n.*971G>A
ENST00000648271.1:c.*2293G>A	ENSP00000497795.1:n.*2293G>A
ENST00000648807.1:c.1674G>A	ENSP00000497472.1:p.Arg558=
ENST00000648960.1:c.1344G>A	ENSP00000497091.1:p.Arg448=
ENST00000649067.1:c.*830G>A	ENSP00000497052.1:n.*830G>A
ENST00000649689.2:c.1827G>A MANE Select	ENSP00000497569.1:p.Arg609=
ENST00000361951.4:c.1827G>A	ENSP00000355086.4:p.Arg609=
ENST00000471476.1:n.649G>A
NM_018122.4:c.1827G>A	NP_060592.2:p.Arg609=
XM_006711427.2:c.1674G>A	XP_006711490.1:p.Arg558=
NM_001365212.1:c.1674G>A	NP_001352141.1:p.Arg558=
NM_018122.5:c.1827G>A MANE Select	NP_060592.2:p.Arg609=