Canonical Allele Identifier: CA2682251024

Gene: GARS1

Linked Data

• gnomAD v4: 7-30626184-CACAGGGTGCCTGTTTGA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30626187_30626203del , CM000669.2:g.30626187_30626203del	GRCh38
NC_000007.13:g.30665803_30665819del , CM000669.1:g.30665803_30665819del	GRCh37
NC_000007.12:g.30632328_30632344del	NCBI36
NG_007942.1:g.36623_36639del , LRG_243:g.36623_36639del

Transcript Alleles

HGVS	Amino-acid change
ENST00000389266.8:c.1614-47_1614-31del MANE Select	ENSP00000373918.3:n.1614-47_1614-31del
ENST00000444666.6:c.1614-47_1614-31del	ENSP00000415447.2:n.1614-47_1614-31del
ENST00000470392.2:n.1704-47_1704-31del
ENST00000485784.2:n.1693-47_1693-31del
ENST00000674616.1:c.*1328-47_*1328-31del	ENSP00000502408.1:n.*1328-47_*1328-31del
ENST00000674643.1:c.*714-47_*714-31del	ENSP00000501636.1:n.*714-47_*714-31del
ENST00000674737.1:c.*952-47_*952-31del	ENSP00000502464.1:n.*952-47_*952-31del
ENST00000674807.1:c.1614-2373_1614-2357del	ENSP00000502814.1:n.1614-2373_1614-2357de...
ENST00000674815.1:c.1245-47_1245-31del	ENSP00000502799.1:n.1245-47_1245-31del
ENST00000674851.1:c.1245-47_1245-31del	ENSP00000502451.1:n.1245-47_1245-31del
ENST00000674969.1:n.3487-47_3487-31del
ENST00000675051.1:c.1413-47_1413-31del	ENSP00000502296.1:n.1413-47_1413-31del
ENST00000675529.1:c.*1484-47_*1484-31del	ENSP00000501655.1:n.*1484-47_*1484-31del
ENST00000675587.1:n.2446-47_2446-31del
ENST00000675651.1:c.1614-47_1614-31del	ENSP00000502513.1:n.1614-47_1614-31del
ENST00000675693.1:c.1446-47_1446-31del	ENSP00000502174.1:n.1446-47_1446-31del
ENST00000675810.1:c.1512-47_1512-31del	ENSP00000502743.1:n.1512-47_1512-31del
ENST00000675859.1:c.1614-2373_1614-2357del	ENSP00000502033.1:n.1614-2373_1614-2357de...
ENST00000675863.1:n.1622-47_1622-31del
ENST00000675886.1:n.7654-47_7654-31del
ENST00000676088.1:c.*1556-47_*1556-31del	ENSP00000501884.1:n.*1556-47_*1556-31del
ENST00000676140.1:c.*559-47_*559-31del	ENSP00000502571.1:n.*559-47_*559-31del
ENST00000676164.1:c.*1065-47_*1065-31del	ENSP00000501986.1:n.*1065-47_*1065-31del
ENST00000676210.1:c.*903-47_*903-31del	ENSP00000502373.1:n.*903-47_*903-31del
ENST00000676259.1:c.*1046-47_*1046-31del	ENSP00000501980.1:n.*1046-47_*1046-31del
ENST00000676403.1:c.1614-47_1614-31del	ENSP00000502681.1:n.1614-47_1614-31del
ENST00000389266.7:c.1614-47_1614-31del	ENSP00000373918.3:n.1614-47_1614-31del
ENST00000444666.5:c.135-47_135-31del	ENSP00000415447.1:n.135-47_135-31del
ENST00000470392.1:n.336-47_336-31del
NM_001316772.1:c.1452-47_1452-31del	NP_001303701.1:n.1452-47_1452-31del
NM_002047.2:c.1614-47_1614-31del , LRG_243t1:c.1614-47_1614-31del	NP_002038.2:n.1614-47_1614-31del
NM_002047.3:c.1614-47_1614-31del	NP_002038.2:n.1614-47_1614-31del
XM_006715686.1:c.1245-47_1245-31del	XP_006715749.1:n.1245-47_1245-31del
XM_006715686.2:c.1245-47_1245-31del	XP_006715749.1:n.1245-47_1245-31del
NM_002047.4:c.1614-47_1614-31del MANE Select	NP_002038.2:n.1614-47_1614-31del