Canonical Allele Identifier: CA352423889

Gene: LARS2

Linked Data

• gnomAD v4: 3-45476583-G-C
• MyVariant Identifiers: chr3:g.45518075G>C (hg19) ; chr3:g.45476583G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45476583G>C , CM000665.2:g.45476583G>C	GRCh38
NC_000003.11:g.45518075G>C , CM000665.1:g.45518075G>C	GRCh37
NC_000003.10:g.45493079G>C	NCBI36
NG_033907.1:g.93001G>C
NG_033907.2:g.93001G>C
NG_033907.3:g.93020G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265537.8:c.974G>C	ENSP00000265537.4:p.Ser325Thr
ENST00000642274.1:c.974G>C	ENSP00000495707.1:p.Ser325Thr
ENST00000645846.2:c.974G>C MANE Select	ENSP00000495093.1:p.Ser325Thr
ENST00000650792.2:c.974G>C	ENSP00000498867.1:p.Ser325Thr
ENST00000651549.1:c.974G>C	ENSP00000499002.1:p.Ser325Thr
ENST00000652135.1:c.*842G>C	ENSP00000499104.1:n.*842G>C
ENST00000265537.7:c.974G>C	ENSP00000265537.3:p.Ser325Thr
ENST00000414984.5:c.845G>C	ENSP00000412893.1:p.Ser282Thr
ENST00000415258.5:c.974G>C	ENSP00000408576.1:p.Ser325Thr
NM_015340.3:c.974G>C	NP_056155.1:p.Ser325Thr
XM_005265006.1:c.974G>C	XP_005265063.1:p.Ser325Thr
XM_011533554.1:c.974G>C	XP_011531856.1:p.Ser325Thr
XM_005265006.2:c.974G>C	XP_005265063.1:p.Ser325Thr
XM_011533554.2:c.974G>C	XP_011531856.1:p.Ser325Thr
XM_017006042.1:c.974G>C	XP_016861531.1:p.Ser325Thr
NM_015340.4:c.974G>C MANE Select	NP_056155.1:p.Ser325Thr
NM_001368263.1:c.974G>C	NP_001355192.1:p.Ser325Thr