Canonical Allele Identifier: CA2038898367
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57511748C= , CM000674.2:g.57511748C= GRCh38
NC_000012.11:g.57905531C= , CM000674.1:g.57905531C= GRCh37
NC_000012.10:g.56191798C= NCBI36
NG_034077.1:g.28796C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1419C= MANE Select ENSP00000262027.5:p.Asp473=
ENST00000262027.9:c.1419C= ENSP00000262027.5:p.Asp473=
ENST00000447721.6:n.1061C=
ENST00000537638.6:c.1419C= ENSP00000446168.2:p.Asp473=
ENST00000545888.6:c.*920C= ENSP00000439307.2:n.*920C=
ENST00000546971.5:n.163C=
ENST00000548944.1:c.134-4747C= ENSP00000449071.1:n.134-4747C=
ENST00000549603.1:n.365C=
ENST00000628866.2:c.*920C= ENSP00000486738.1:n.*920C=
NM_004990.3:c.1419C= NP_004981.2:p.Asp473=
XM_006719398.2:c.717C= XP_006719461.1:p.Asp239=
XM_011538353.1:c.1419C= XP_011536655.1:p.Asp473=
XM_006719398.4:c.717C= XP_006719461.1:p.Asp239=
XR_001748704.2:n.1442C=
XR_002957327.1:n.1366C=
NM_004990.4:c.1419C= MANE Select NP_004981.2:p.Asp473=