Canonical Allele Identifier: CA385461508

Gene: MARS1

Linked Data

• dbSNP Id: rs1441274721
• gnomAD v3: 12-57511795-G-A
• gnomAD v4: 12-57511795-G-A
• MyVariant Identifiers: chr12:g.57905578G>A (hg19) ; chr12:g.57511795G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57511795G>A , CM000674.2:g.57511795G>A	GRCh38
NC_000012.11:g.57905578G>A , CM000674.1:g.57905578G>A	GRCh37
NC_000012.10:g.56191845G>A	NCBI36
NG_034077.1:g.28843G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1466G>A MANE Select	ENSP00000262027.5:p.Gly489Asp
ENST00000262027.9:c.1466G>A	ENSP00000262027.5:p.Gly489Asp
ENST00000447721.6:n.1108G>A
ENST00000537638.6:c.1466G>A	ENSP00000446168.2:p.Gly489Asp
ENST00000545888.6:c.*967G>A	ENSP00000439307.2:n.*967G>A
ENST00000546971.5:n.210G>A
ENST00000548630.1:n.27G>A
ENST00000548944.1:c.134-4700G>A	ENSP00000449071.1:n.134-4700G>A
ENST00000628866.2:c.*967G>A	ENSP00000486738.1:n.*967G>A
NM_004990.3:c.1466G>A	NP_004981.2:p.Gly489Asp
XM_006719398.2:c.764G>A	XP_006719461.1:p.Gly255Asp
XM_011538353.1:c.1466G>A	XP_011536655.1:p.Gly489Asp
XM_006719398.4:c.764G>A	XP_006719461.1:p.Gly255Asp
XR_001748704.2:n.1489G>A
XR_002957327.1:n.1413G>A
NM_004990.4:c.1466G>A MANE Select	NP_004981.2:p.Gly489Asp