Canonical Allele Identifier: CA237768119
Gene: MARS1 HGNC NCBI

Linked Data

dbSNP Id: rs911280490

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57511865C>A , CM000674.2:g.57511865C>A GRCh38
NC_000012.11:g.57905648C>A , CM000674.1:g.57905648C>A GRCh37
NC_000012.10:g.56191915C>A NCBI36
NG_034077.1:g.28913C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1536C>A MANE Select ENSP00000262027.5:p.Asp512Glu
ENST00000262027.9:c.1536C>A ENSP00000262027.5:p.Asp512Glu
ENST00000447721.6:n.1178C>A
ENST00000537638.6:c.1536C>A ENSP00000446168.2:p.Asp512Glu
ENST00000545888.6:c.*1037C>A ENSP00000439307.2:n.*1037C>A
ENST00000546971.5:n.280C>A
ENST00000548630.1:n.97C>A
ENST00000548944.1:c.134-4630C>A ENSP00000449071.1:n.134-4630C>A
ENST00000549048.1:n.69C>A
ENST00000628866.2:c.*1037C>A ENSP00000486738.1:n.*1037C>A
NM_004990.3:c.1536C>A NP_004981.2:p.Asp512Glu
XM_006719398.2:c.834C>A XP_006719461.1:p.Asp278Glu
XM_011538353.1:c.1536C>A XP_011536655.1:p.Asp512Glu
XM_006719398.4:c.834C>A XP_006719461.1:p.Asp278Glu
XR_001748704.2:n.1559C>A
XR_002957327.1:n.1483C>A
NM_004990.4:c.1536C>A MANE Select NP_004981.2:p.Asp512Glu