Canonical Allele Identifier: CA367124479

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30649282T>C (hg19) ; chr7:g.30609666T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30609666T>C , CM000669.2:g.30609666T>C	GRCh38
NC_000007.13:g.30649282T>C , CM000669.1:g.30649282T>C	GRCh37
NC_000007.12:g.30615807T>C	NCBI36
NG_007942.1:g.20102T>C , LRG_243:g.20102T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.817T>C MANE Select	ENSP00000373918.3:p.Ser273Pro
ENST00000444666.6:c.817T>C	ENSP00000415447.2:p.Ser273Pro
ENST00000470392.2:n.907T>C
ENST00000478124.6:n.880T>C
ENST00000485784.2:n.896T>C
ENST00000674616.1:c.*531T>C	ENSP00000502408.1:n.*531T>C
ENST00000674643.1:c.817T>C	ENSP00000501636.1:p.Ser273Pro
ENST00000674734.1:n.1313T>C
ENST00000674737.1:c.*155T>C	ENSP00000502464.1:n.*155T>C
ENST00000674807.1:c.817T>C	ENSP00000502814.1:p.Ser273Pro
ENST00000674815.1:c.448T>C	ENSP00000502799.1:p.Ser150Pro
ENST00000674851.1:c.448T>C	ENSP00000502451.1:p.Ser150Pro
ENST00000674969.1:n.2690T>C
ENST00000675051.1:c.616T>C	ENSP00000502296.1:p.Ser206Pro
ENST00000675529.1:c.*687T>C	ENSP00000501655.1:n.*687T>C
ENST00000675587.1:n.833T>C
ENST00000675651.1:c.817T>C	ENSP00000502513.1:p.Ser273Pro
ENST00000675693.1:c.649T>C	ENSP00000502174.1:p.Ser217Pro
ENST00000675810.1:c.715T>C	ENSP00000502743.1:p.Ser239Pro
ENST00000675859.1:c.817T>C	ENSP00000502033.1:p.Ser273Pro
ENST00000675863.1:n.825T>C
ENST00000675886.1:n.6857T>C
ENST00000676088.1:c.*759T>C	ENSP00000501884.1:n.*759T>C
ENST00000676140.1:c.817T>C	ENSP00000502571.1:p.Ser273Pro
ENST00000676164.1:c.*268T>C	ENSP00000501986.1:n.*268T>C
ENST00000676210.1:c.*106T>C	ENSP00000502373.1:n.*106T>C
ENST00000676259.1:c.*249T>C	ENSP00000501980.1:n.*249T>C
ENST00000676403.1:c.817T>C	ENSP00000502681.1:p.Ser273Pro
ENST00000389266.7:c.817T>C	ENSP00000373918.3:p.Ser273Pro
ENST00000478124.5:n.855T>C
NM_001316772.1:c.655T>C	NP_001303701.1:p.Ser219Pro
NM_002047.2:c.817T>C , LRG_243t1:c.817T>C	NP_002038.2:p.Ser273Pro
NM_002047.3:c.817T>C	NP_002038.2:p.Ser273Pro
XM_006715686.1:c.448T>C	XP_006715749.1:p.Ser150Pro
XM_006715686.2:c.448T>C	XP_006715749.1:p.Ser150Pro
NM_002047.4:c.817T>C MANE Select	NP_002038.2:p.Ser273Pro