Canonical Allele Identifier: CA367124547

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30649301A>C (hg19) ; chr7:g.30609685A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30609685A>C , CM000669.2:g.30609685A>C	GRCh38
NC_000007.13:g.30649301A>C , CM000669.1:g.30649301A>C	GRCh37
NC_000007.12:g.30615826A>C	NCBI36
NG_007942.1:g.20121A>C , LRG_243:g.20121A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.836A>C MANE Select	ENSP00000373918.3:p.Asn279Thr
ENST00000444666.6:c.836A>C	ENSP00000415447.2:p.Asn279Thr
ENST00000470392.2:n.926A>C
ENST00000478124.6:n.899A>C
ENST00000485784.2:n.915A>C
ENST00000674616.1:c.*550A>C	ENSP00000502408.1:n.*550A>C
ENST00000674643.1:c.836A>C	ENSP00000501636.1:p.Asn279Thr
ENST00000674734.1:n.1332A>C
ENST00000674737.1:c.*174A>C	ENSP00000502464.1:n.*174A>C
ENST00000674807.1:c.836A>C	ENSP00000502814.1:p.Asn279Thr
ENST00000674815.1:c.467A>C	ENSP00000502799.1:p.Asn156Thr
ENST00000674851.1:c.467A>C	ENSP00000502451.1:p.Asn156Thr
ENST00000674969.1:n.2709A>C
ENST00000675051.1:c.635A>C	ENSP00000502296.1:p.Asn212Thr
ENST00000675529.1:c.*706A>C	ENSP00000501655.1:n.*706A>C
ENST00000675587.1:n.852A>C
ENST00000675651.1:c.836A>C	ENSP00000502513.1:p.Asn279Thr
ENST00000675693.1:c.668A>C	ENSP00000502174.1:p.Asn223Thr
ENST00000675810.1:c.734A>C	ENSP00000502743.1:p.Asn245Thr
ENST00000675859.1:c.836A>C	ENSP00000502033.1:p.Asn279Thr
ENST00000675863.1:n.844A>C
ENST00000675886.1:n.6876A>C
ENST00000676088.1:c.*778A>C	ENSP00000501884.1:n.*778A>C
ENST00000676140.1:c.836A>C	ENSP00000502571.1:p.Asn279Thr
ENST00000676164.1:c.*287A>C	ENSP00000501986.1:n.*287A>C
ENST00000676210.1:c.*125A>C	ENSP00000502373.1:n.*125A>C
ENST00000676259.1:c.*268A>C	ENSP00000501980.1:n.*268A>C
ENST00000676403.1:c.836A>C	ENSP00000502681.1:p.Asn279Thr
ENST00000389266.7:c.836A>C	ENSP00000373918.3:p.Asn279Thr
ENST00000478124.5:n.874A>C
NM_001316772.1:c.674A>C	NP_001303701.1:p.Asn225Thr
NM_002047.2:c.836A>C , LRG_243t1:c.836A>C	NP_002038.2:p.Asn279Thr
NM_002047.3:c.836A>C	NP_002038.2:p.Asn279Thr
XM_006715686.1:c.467A>C	XP_006715749.1:p.Asn156Thr
XM_006715686.2:c.467A>C	XP_006715749.1:p.Asn156Thr
NM_002047.4:c.836A>C MANE Select	NP_002038.2:p.Asn279Thr