Canonical Allele Identifier: CA2038898504
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57512077G= , CM000674.2:g.57512077G= GRCh38
NC_000012.11:g.57905860G= , CM000674.1:g.57905860G= GRCh37
NC_000012.10:g.56192127G= NCBI36
NG_034077.1:g.29125G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1609G= MANE Select ENSP00000262027.5:p.Glu537=
ENST00000262027.9:c.1609G= ENSP00000262027.5:p.Glu537=
ENST00000447721.6:n.1251G=
ENST00000537638.6:c.1609G= ENSP00000446168.2:p.Glu537=
ENST00000545888.6:c.*1110G= ENSP00000439307.2:n.*1110G=
ENST00000546971.5:n.353G=
ENST00000548630.1:n.170G=
ENST00000548944.1:c.134-4418G= ENSP00000449071.1:n.134-4418G=
ENST00000549048.1:n.142G=
ENST00000628866.2:c.*1110G= ENSP00000486738.1:n.*1110G=
NM_004990.3:c.1609G= NP_004981.2:p.Glu537=
XM_006719398.2:c.907G= XP_006719461.1:p.Glu303=
XM_011538353.1:c.1609G= XP_011536655.1:p.Glu537=
XM_006719398.4:c.907G= XP_006719461.1:p.Glu303=
XR_001748704.2:n.1632G=
XR_002957327.1:n.1556G=
NM_004990.4:c.1609G= MANE Select NP_004981.2:p.Glu537=