Canonical Allele Identifier: CA2038898395
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57511818C= , CM000674.2:g.57511818C= GRCh38
NC_000012.11:g.57905601C= , CM000674.1:g.57905601C= GRCh37
NC_000012.10:g.56191868C= NCBI36
NG_034077.1:g.28866C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1489C= MANE Select ENSP00000262027.5:p.Arg497=
ENST00000262027.9:c.1489C= ENSP00000262027.5:p.Arg497=
ENST00000447721.6:n.1131C=
ENST00000537638.6:c.1489C= ENSP00000446168.2:p.Arg497=
ENST00000545888.6:c.*990C= ENSP00000439307.2:n.*990C=
ENST00000546971.5:n.233C=
ENST00000548630.1:n.50C=
ENST00000548944.1:c.134-4677C= ENSP00000449071.1:n.134-4677C=
ENST00000549048.1:n.22C=
ENST00000628866.2:c.*990C= ENSP00000486738.1:n.*990C=
NM_004990.3:c.1489C= NP_004981.2:p.Arg497=
XM_006719398.2:c.787C= XP_006719461.1:p.Arg263=
XM_011538353.1:c.1489C= XP_011536655.1:p.Arg497=
XM_006719398.4:c.787C= XP_006719461.1:p.Arg263=
XR_001748704.2:n.1512C=
XR_002957327.1:n.1436C=
NM_004990.4:c.1489C= MANE Select NP_004981.2:p.Arg497=