Canonical Allele Identifier: CA2038898357
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57511724G= , CM000674.2:g.57511724G= GRCh38
NC_000012.11:g.57905507G= , CM000674.1:g.57905507G= GRCh37
NC_000012.10:g.56191774G= NCBI36
NG_034077.1:g.28772G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1395G= MANE Select ENSP00000262027.5:p.Leu465=
ENST00000262027.9:c.1395G= ENSP00000262027.5:p.Leu465=
ENST00000447721.6:n.1037G=
ENST00000537638.6:c.1395G= ENSP00000446168.2:p.Leu465=
ENST00000545888.6:c.*896G= ENSP00000439307.2:n.*896G=
ENST00000546971.5:n.139G=
ENST00000548944.1:c.134-4771G= ENSP00000449071.1:n.134-4771G=
ENST00000549603.1:n.341G=
ENST00000628866.2:c.*896G= ENSP00000486738.1:n.*896G=
NM_004990.3:c.1395G= NP_004981.2:p.Leu465=
XM_006719398.2:c.693G= XP_006719461.1:p.Leu231=
XM_011538353.1:c.1395G= XP_011536655.1:p.Leu465=
XM_006719398.4:c.693G= XP_006719461.1:p.Leu231=
XR_001748704.2:n.1418G=
XR_002957327.1:n.1342G=
NM_004990.4:c.1395G= MANE Select NP_004981.2:p.Leu465=