Canonical Allele Identifier: CA1697807383

Gene: GARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30609553_30609555delinsCTT , CM000669.2:g.30609553_30609555delinsCTT	GRCh38
NC_000007.13:g.30649169_30649171delinsCTT , CM000669.1:g.30649169_30649171delinsCTT	GRCh37
NC_000007.12:g.30615694_30615696delinsCTT	NCBI36
NG_007942.1:g.19989_19991delinsCTT , LRG_243:g.19989_19991delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.736-32_736-30delinsCTT MANE Select	ENSP00000373918.3:n.736-32_736-30delinsCTT
ENST00000444666.6:c.736-32_736-30delinsCTT	ENSP00000415447.2:n.736-32_736-30delinsCTT
ENST00000470392.2:n.826-32_826-30delinsCTT
ENST00000478124.6:n.799-32_799-30delinsCTT
ENST00000485784.2:n.815-32_815-30delinsCTT
ENST00000674616.1:c.*450-32_*450-30delinsCTT	ENSP00000502408.1:n.*450-32_*450-30delinsCTT
ENST00000674643.1:c.736-32_736-30delinsCTT	ENSP00000501636.1:n.736-32_736-30delinsCTT
ENST00000674734.1:n.1232-32_1232-30delinsCTT
ENST00000674737.1:c.*74-32_*74-30delinsCTT	ENSP00000502464.1:n.*74-32_*74-30delinsCTT
ENST00000674807.1:c.736-32_736-30delinsCTT	ENSP00000502814.1:n.736-32_736-30delinsCTT
ENST00000674815.1:c.367-32_367-30delinsCTT	ENSP00000502799.1:n.367-32_367-30delinsCTT
ENST00000674851.1:c.367-32_367-30delinsCTT	ENSP00000502451.1:n.367-32_367-30delinsCTT
ENST00000674969.1:n.2609-32_2609-30delinsCTT
ENST00000675051.1:c.535-32_535-30delinsCTT	ENSP00000502296.1:n.535-32_535-30delinsCTT
ENST00000675529.1:c.*606-32_*606-30delinsCTT	ENSP00000501655.1:n.*606-32_*606-30delinsCTT
ENST00000675587.1:n.752-32_752-30delinsCTT
ENST00000675651.1:c.736-32_736-30delinsCTT	ENSP00000502513.1:n.736-32_736-30delinsCTT
ENST00000675693.1:c.568-32_568-30delinsCTT	ENSP00000502174.1:n.568-32_568-30delinsCTT
ENST00000675810.1:c.634-32_634-30delinsCTT	ENSP00000502743.1:n.634-32_634-30delinsCTT
ENST00000675859.1:c.736-32_736-30delinsCTT	ENSP00000502033.1:n.736-32_736-30delinsCTT
ENST00000675863.1:n.744-32_744-30delinsCTT
ENST00000675886.1:n.6744_6746delinsCTT
ENST00000676088.1:c.*678-32_*678-30delinsCTT	ENSP00000501884.1:n.*678-32_*678-30delinsCTT
ENST00000676140.1:c.736-32_736-30delinsCTT	ENSP00000502571.1:n.736-32_736-30delinsCTT
ENST00000676164.1:c.*187-32_*187-30delinsCTT	ENSP00000501986.1:n.*187-32_*187-30delinsCTT
ENST00000676210.1:c.*25-32_*25-30delinsCTT	ENSP00000502373.1:n.*25-32_*25-30delinsCTT
ENST00000676259.1:c.*168-32_*168-30delinsCTT	ENSP00000501980.1:n.*168-32_*168-30delinsCTT
ENST00000676403.1:c.736-32_736-30delinsCTT	ENSP00000502681.1:n.736-32_736-30delinsCTT
ENST00000389266.7:c.736-32_736-30delinsCTT	ENSP00000373918.3:n.736-32_736-30delinsCTT
ENST00000478124.5:n.774-32_774-30delinsCTT
NM_001316772.1:c.574-32_574-30delinsCTT	NP_001303701.1:n.574-32_574-30delinsCTT
NM_002047.2:c.736-32_736-30delinsCTT , LRG_243t1:c.736-32_736-30delinsCTT	NP_002038.2:n.736-32_736-30delinsCTT
NM_002047.3:c.736-32_736-30delinsCTT	NP_002038.2:n.736-32_736-30delinsCTT
XM_006715686.1:c.367-32_367-30delinsCTT	XP_006715749.1:n.367-32_367-30delinsCTT
XM_006715686.2:c.367-32_367-30delinsCTT	XP_006715749.1:n.367-32_367-30delinsCTT
NM_002047.4:c.736-32_736-30delinsCTT MANE Select	NP_002038.2:n.736-32_736-30delinsCTT