Canonical Allele Identifier: CA454246826

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30649299T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30609683T>C , CM000669.2:g.30609683T>C	GRCh38
NC_000007.13:g.30649299T>C , CM000669.1:g.30649299T>C	GRCh37
NC_000007.12:g.30615824T>C	NCBI36
NG_007942.1:g.20119T>C , LRG_243:g.20119T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.834T>C MANE Select	ENSP00000373918.3:p.Phe278=
ENST00000444666.6:c.834T>C	ENSP00000415447.2:p.Phe278=
ENST00000470392.2:n.924T>C
ENST00000478124.6:n.897T>C
ENST00000485784.2:n.913T>C
ENST00000674616.1:c.*548T>C	ENSP00000502408.1:n.*548T>C
ENST00000674643.1:c.834T>C	ENSP00000501636.1:p.Phe278=
ENST00000674734.1:n.1330T>C
ENST00000674737.1:c.*172T>C	ENSP00000502464.1:n.*172T>C
ENST00000674807.1:c.834T>C	ENSP00000502814.1:p.Phe278=
ENST00000674815.1:c.465T>C	ENSP00000502799.1:p.Phe155=
ENST00000674851.1:c.465T>C	ENSP00000502451.1:p.Phe155=
ENST00000674969.1:n.2707T>C
ENST00000675051.1:c.633T>C	ENSP00000502296.1:p.Phe211=
ENST00000675529.1:c.*704T>C	ENSP00000501655.1:n.*704T>C
ENST00000675587.1:n.850T>C
ENST00000675651.1:c.834T>C	ENSP00000502513.1:p.Phe278=
ENST00000675693.1:c.666T>C	ENSP00000502174.1:p.Phe222=
ENST00000675810.1:c.732T>C	ENSP00000502743.1:p.Phe244=
ENST00000675859.1:c.834T>C	ENSP00000502033.1:p.Phe278=
ENST00000675863.1:n.842T>C
ENST00000675886.1:n.6874T>C
ENST00000676088.1:c.*776T>C	ENSP00000501884.1:n.*776T>C
ENST00000676140.1:c.834T>C	ENSP00000502571.1:p.Phe278=
ENST00000676164.1:c.*285T>C	ENSP00000501986.1:n.*285T>C
ENST00000676210.1:c.*123T>C	ENSP00000502373.1:n.*123T>C
ENST00000676259.1:c.*266T>C	ENSP00000501980.1:n.*266T>C
ENST00000676403.1:c.834T>C	ENSP00000502681.1:p.Phe278=
ENST00000389266.7:c.834T>C	ENSP00000373918.3:p.Phe278=
ENST00000478124.5:n.872T>C
NM_001316772.1:c.672T>C	NP_001303701.1:p.Phe224=
NM_002047.2:c.834T>C , LRG_243t1:c.834T>C	NP_002038.2:p.Phe278=
NM_002047.3:c.834T>C	NP_002038.2:p.Phe278=
XM_006715686.1:c.465T>C	XP_006715749.1:p.Phe155=
XM_006715686.2:c.465T>C	XP_006715749.1:p.Phe155=
NM_002047.4:c.834T>C MANE Select	NP_002038.2:p.Phe278=