Canonical Allele Identifier: CA2038903452
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57512811A= , CM000674.2:g.57512811A= GRCh38
NC_000012.11:g.57906594A= , CM000674.1:g.57906594A= GRCh37
NC_000012.10:g.56192861A= NCBI36
NG_034077.1:g.29859A=

Transcript Alleles

HGVS Amino-acid change
ENST00000262027.10:c.1814A= MANE Select ENSP00000262027.5:p.Asp605=
ENST00000262027.9:c.1814A= ENSP00000262027.5:p.Asp605=
ENST00000537638.6:c.*106A= ENSP00000446168.2:n.*106A=
ENST00000545888.6:c.*1315A= ENSP00000439307.2:n.*1315A=
ENST00000546971.5:n.558A=
ENST00000548202.5:n.321A=
ENST00000548944.1:c.134-3684A= ENSP00000449071.1:n.134-3684A=
ENST00000549048.1:n.479A=
ENST00000628866.2:c.*1315A= ENSP00000486738.1:n.*1315A=
NM_004990.3:c.1814A= NP_004981.2:p.Asp605=
XM_006719398.2:c.1112A= XP_006719461.1:p.Asp371=
XM_011538353.1:c.*106A= XP_011536655.1:n.*106A=
XM_006719398.4:c.1112A= XP_006719461.1:p.Asp371=
XR_001748704.2:n.1770A=
XR_002957327.1:n.1761A=
NM_004990.4:c.1814A= MANE Select NP_004981.2:p.Asp605=