Canonical Allele Identifier: CA385460884
Gene: MARS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57511701G>A , CM000674.2:g.57511701G>A GRCh38
NC_000012.11:g.57905484G>A , CM000674.1:g.57905484G>A GRCh37
NC_000012.10:g.56191751G>A NCBI36
NG_034077.1:g.28749G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1372G>A MANE Select ENSP00000262027.5:p.Glu458Lys
ENST00000262027.9:c.1372G>A ENSP00000262027.5:p.Glu458Lys
ENST00000447721.6:n.1014G>A
ENST00000537638.6:c.1372G>A ENSP00000446168.2:p.Glu458Lys
ENST00000545888.6:c.*873G>A ENSP00000439307.2:n.*873G>A
ENST00000546971.5:n.116G>A
ENST00000548944.1:c.134-4794G>A ENSP00000449071.1:n.134-4794G>A
ENST00000549603.1:n.318G>A
ENST00000628866.2:c.*873G>A ENSP00000486738.1:n.*873G>A
NM_004990.3:c.1372G>A NP_004981.2:p.Glu458Lys
XM_006719398.2:c.670G>A XP_006719461.1:p.Glu224Lys
XM_011538353.1:c.1372G>A XP_011536655.1:p.Glu458Lys
XM_006719398.4:c.670G>A XP_006719461.1:p.Glu224Lys
XR_001748704.2:n.1395G>A
XR_002957327.1:n.1319G>A
NM_004990.4:c.1372G>A MANE Select NP_004981.2:p.Glu458Lys