Canonical Allele Identifier: CA2649165103

Gene: DARS2

Linked Data

• gnomAD v4: 1-173857429-AAAGTTTTCTACAACTTTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173857431_173857448del , CM000663.2:g.173857431_173857448del	GRCh38
NC_000001.10:g.173826569_173826586del , CM000663.1:g.173826569_173826586del	GRCh37
NC_000001.9:g.172093192_172093209del	NCBI36
NG_016138.1:g.37773_37790del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471476.2:c.*1330-87_*1330-70del	ENSP00000497663.1:n.*1330-87_*1330-70del
ENST00000647645.1:c.1688-87_1688-70del	ENSP00000497450.1:n.1688-87_1688-70del
ENST00000647730.1:c.*1441-87_*1441-70del	ENSP00000497781.1:n.*1441-87_*1441-70del
ENST00000647788.1:c.*895-87_*895-70del	ENSP00000497769.1:n.*895-87_*895-70del
ENST00000648271.1:c.*2130_*2147del	ENSP00000497795.1:n.*2130_*2147del
ENST00000648807.1:c.1598-87_1598-70del	ENSP00000497472.1:n.1598-87_1598-70del
ENST00000648960.1:c.1268-87_1268-70del	ENSP00000497091.1:n.1268-87_1268-70del
ENST00000649067.1:c.*667_*684del	ENSP00000497052.1:n.*667_*684del
ENST00000649689.2:c.1751-87_1751-70del MANE Select	ENSP00000497569.1:n.1751-87_1751-70del
ENST00000361951.4:c.1751-87_1751-70del	ENSP00000355086.4:n.1751-87_1751-70del
ENST00000471476.1:n.573-87_573-70del
NM_018122.4:c.1751-87_1751-70del	NP_060592.2:n.1751-87_1751-70del
XM_006711427.2:c.1598-87_1598-70del	XP_006711490.1:n.1598-87_1598-70del
NM_001365212.1:c.1598-87_1598-70del	NP_001352141.1:n.1598-87_1598-70del
NM_018122.5:c.1751-87_1751-70del MANE Select	NP_060592.2:n.1751-87_1751-70del