Canonical Allele Identifier: CA367125031

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30651776C>T (hg19) ; chr7:g.30612160C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30612160C>T , CM000669.2:g.30612160C>T	GRCh38
NC_000007.13:g.30651776C>T , CM000669.1:g.30651776C>T	GRCh37
NC_000007.12:g.30618301C>T	NCBI36
NG_007942.1:g.22596C>T , LRG_243:g.22596C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.946C>T MANE Select	ENSP00000373918.3:p.Gln316Ter
ENST00000444666.6:c.946C>T	ENSP00000415447.2:p.Gln316Ter
ENST00000470392.2:n.1036C>T
ENST00000478124.6:n.1009C>T
ENST00000485784.2:n.1025C>T
ENST00000674616.1:c.*660C>T	ENSP00000502408.1:n.*660C>T
ENST00000674643.1:c.946C>T	ENSP00000501636.1:p.Gln316Ter
ENST00000674734.1:n.1442C>T
ENST00000674737.1:c.*284C>T	ENSP00000502464.1:n.*284C>T
ENST00000674807.1:c.946C>T	ENSP00000502814.1:p.Gln316Ter
ENST00000674815.1:c.577C>T	ENSP00000502799.1:p.Gln193Ter
ENST00000674851.1:c.577C>T	ENSP00000502451.1:p.Gln193Ter
ENST00000674969.1:n.2819C>T
ENST00000675051.1:c.745C>T	ENSP00000502296.1:p.Gln249Ter
ENST00000675529.1:c.*816C>T	ENSP00000501655.1:n.*816C>T
ENST00000675587.1:n.962C>T
ENST00000675651.1:c.946C>T	ENSP00000502513.1:p.Gln316Ter
ENST00000675693.1:c.778C>T	ENSP00000502174.1:p.Gln260Ter
ENST00000675810.1:c.844C>T	ENSP00000502743.1:p.Gln282Ter
ENST00000675859.1:c.946C>T	ENSP00000502033.1:p.Gln316Ter
ENST00000675863.1:n.954C>T
ENST00000675886.1:n.6986C>T
ENST00000676088.1:c.*888C>T	ENSP00000501884.1:n.*888C>T
ENST00000676140.1:c.946C>T	ENSP00000502571.1:p.Gln316Ter
ENST00000676164.1:c.*397C>T	ENSP00000501986.1:n.*397C>T
ENST00000676210.1:c.*235C>T	ENSP00000502373.1:n.*235C>T
ENST00000676259.1:c.*378C>T	ENSP00000501980.1:n.*378C>T
ENST00000676403.1:c.946C>T	ENSP00000502681.1:p.Gln316Ter
ENST00000389266.7:c.946C>T	ENSP00000373918.3:p.Gln316Ter
ENST00000478124.5:n.984C>T
NM_001316772.1:c.784C>T	NP_001303701.1:p.Gln262Ter
NM_002047.2:c.946C>T , LRG_243t1:c.946C>T	NP_002038.2:p.Gln316Ter
NM_002047.3:c.946C>T	NP_002038.2:p.Gln316Ter
XM_006715686.1:c.577C>T	XP_006715749.1:p.Gln193Ter
XM_006715686.2:c.577C>T	XP_006715749.1:p.Gln193Ter
NM_002047.4:c.946C>T MANE Select	NP_002038.2:p.Gln316Ter