Canonical Allele Identifier: CA367124869

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30651731G>T (hg19) ; chr7:g.30612115G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30612115G>T , CM000669.2:g.30612115G>T	GRCh38
NC_000007.13:g.30651731G>T , CM000669.1:g.30651731G>T	GRCh37
NC_000007.12:g.30618256G>T	NCBI36
NG_007942.1:g.22551G>T , LRG_243:g.22551G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.901G>T MANE Select	ENSP00000373918.3:p.Ala301Ser
ENST00000444666.6:c.901G>T	ENSP00000415447.2:p.Ala301Ser
ENST00000470392.2:n.991G>T
ENST00000478124.6:n.964G>T
ENST00000485784.2:n.980G>T
ENST00000674616.1:c.*615G>T	ENSP00000502408.1:n.*615G>T
ENST00000674643.1:c.901G>T	ENSP00000501636.1:p.Ala301Ser
ENST00000674734.1:n.1397G>T
ENST00000674737.1:c.*239G>T	ENSP00000502464.1:n.*239G>T
ENST00000674807.1:c.901G>T	ENSP00000502814.1:p.Ala301Ser
ENST00000674815.1:c.532G>T	ENSP00000502799.1:p.Ala178Ser
ENST00000674851.1:c.532G>T	ENSP00000502451.1:p.Ala178Ser
ENST00000674969.1:n.2774G>T
ENST00000675051.1:c.700G>T	ENSP00000502296.1:p.Ala234Ser
ENST00000675529.1:c.*771G>T	ENSP00000501655.1:n.*771G>T
ENST00000675587.1:n.917G>T
ENST00000675651.1:c.901G>T	ENSP00000502513.1:p.Ala301Ser
ENST00000675693.1:c.733G>T	ENSP00000502174.1:p.Ala245Ser
ENST00000675810.1:c.799G>T	ENSP00000502743.1:p.Ala267Ser
ENST00000675859.1:c.901G>T	ENSP00000502033.1:p.Ala301Ser
ENST00000675863.1:n.909G>T
ENST00000675886.1:n.6941G>T
ENST00000676088.1:c.*843G>T	ENSP00000501884.1:n.*843G>T
ENST00000676140.1:c.901G>T	ENSP00000502571.1:p.Ala301Ser
ENST00000676164.1:c.*352G>T	ENSP00000501986.1:n.*352G>T
ENST00000676210.1:c.*190G>T	ENSP00000502373.1:n.*190G>T
ENST00000676259.1:c.*333G>T	ENSP00000501980.1:n.*333G>T
ENST00000676403.1:c.901G>T	ENSP00000502681.1:p.Ala301Ser
ENST00000389266.7:c.901G>T	ENSP00000373918.3:p.Ala301Ser
ENST00000478124.5:n.939G>T
NM_001316772.1:c.739G>T	NP_001303701.1:p.Ala247Ser
NM_002047.2:c.901G>T , LRG_243t1:c.901G>T	NP_002038.2:p.Ala301Ser
NM_002047.3:c.901G>T	NP_002038.2:p.Ala301Ser
XM_006715686.1:c.532G>T	XP_006715749.1:p.Ala178Ser
XM_006715686.2:c.532G>T	XP_006715749.1:p.Ala178Ser
NM_002047.4:c.901G>T MANE Select	NP_002038.2:p.Ala301Ser