Canonical Allele Identifier: CA2038903496
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57512827G= , CM000674.2:g.57512827G= GRCh38
NC_000012.11:g.57906610G= , CM000674.1:g.57906610G= GRCh37
NC_000012.10:g.56192877G= NCBI36
NG_034077.1:g.29875G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262027.10:c.1830G= MANE Select ENSP00000262027.5:p.Thr610=
ENST00000262027.9:c.1830G= ENSP00000262027.5:p.Thr610=
ENST00000537638.6:c.*122G= ENSP00000446168.2:n.*122G=
ENST00000545888.6:c.*1331G= ENSP00000439307.2:n.*1331G=
ENST00000546971.5:n.574G=
ENST00000548202.5:n.337G=
ENST00000548944.1:c.134-3668G= ENSP00000449071.1:n.134-3668G=
ENST00000549048.1:n.495G=
ENST00000628866.2:c.*1331G= ENSP00000486738.1:n.*1331G=
NM_004990.3:c.1830G= NP_004981.2:p.Thr610=
XM_006719398.2:c.1128G= XP_006719461.1:p.Thr376=
XM_011538353.1:c.*122G= XP_011536655.1:n.*122G=
XM_006719398.4:c.1128G= XP_006719461.1:p.Thr376=
XR_001748704.2:n.1786G=
XR_002957327.1:n.1777G=
NM_004990.4:c.1830G= MANE Select NP_004981.2:p.Thr610=