Canonical Allele Identifier: CA367124958

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30651756A>C (hg19) ; chr7:g.30612140A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30612140A>C , CM000669.2:g.30612140A>C	GRCh38
NC_000007.13:g.30651756A>C , CM000669.1:g.30651756A>C	GRCh37
NC_000007.12:g.30618281A>C	NCBI36
NG_007942.1:g.22576A>C , LRG_243:g.22576A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.926A>C MANE Select	ENSP00000373918.3:p.Lys309Thr
ENST00000444666.6:c.926A>C	ENSP00000415447.2:p.Lys309Thr
ENST00000470392.2:n.1016A>C
ENST00000478124.6:n.989A>C
ENST00000485784.2:n.1005A>C
ENST00000674616.1:c.*640A>C	ENSP00000502408.1:n.*640A>C
ENST00000674643.1:c.926A>C	ENSP00000501636.1:p.Lys309Thr
ENST00000674734.1:n.1422A>C
ENST00000674737.1:c.*264A>C	ENSP00000502464.1:n.*264A>C
ENST00000674807.1:c.926A>C	ENSP00000502814.1:p.Lys309Thr
ENST00000674815.1:c.557A>C	ENSP00000502799.1:p.Lys186Thr
ENST00000674851.1:c.557A>C	ENSP00000502451.1:p.Lys186Thr
ENST00000674969.1:n.2799A>C
ENST00000675051.1:c.725A>C	ENSP00000502296.1:p.Lys242Thr
ENST00000675529.1:c.*796A>C	ENSP00000501655.1:n.*796A>C
ENST00000675587.1:n.942A>C
ENST00000675651.1:c.926A>C	ENSP00000502513.1:p.Lys309Thr
ENST00000675693.1:c.758A>C	ENSP00000502174.1:p.Lys253Thr
ENST00000675810.1:c.824A>C	ENSP00000502743.1:p.Lys275Thr
ENST00000675859.1:c.926A>C	ENSP00000502033.1:p.Lys309Thr
ENST00000675863.1:n.934A>C
ENST00000675886.1:n.6966A>C
ENST00000676088.1:c.*868A>C	ENSP00000501884.1:n.*868A>C
ENST00000676140.1:c.926A>C	ENSP00000502571.1:p.Lys309Thr
ENST00000676164.1:c.*377A>C	ENSP00000501986.1:n.*377A>C
ENST00000676210.1:c.*215A>C	ENSP00000502373.1:n.*215A>C
ENST00000676259.1:c.*358A>C	ENSP00000501980.1:n.*358A>C
ENST00000676403.1:c.926A>C	ENSP00000502681.1:p.Lys309Thr
ENST00000389266.7:c.926A>C	ENSP00000373918.3:p.Lys309Thr
ENST00000478124.5:n.964A>C
NM_001316772.1:c.764A>C	NP_001303701.1:p.Lys255Thr
NM_002047.2:c.926A>C , LRG_243t1:c.926A>C	NP_002038.2:p.Lys309Thr
NM_002047.3:c.926A>C	NP_002038.2:p.Lys309Thr
XM_006715686.1:c.557A>C	XP_006715749.1:p.Lys186Thr
XM_006715686.2:c.557A>C	XP_006715749.1:p.Lys186Thr
NM_002047.4:c.926A>C MANE Select	NP_002038.2:p.Lys309Thr