Canonical Allele Identifier: CA2038898385
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57511791G= , CM000674.2:g.57511791G= GRCh38
NC_000012.11:g.57905574G= , CM000674.1:g.57905574G= GRCh37
NC_000012.10:g.56191841G= NCBI36
NG_034077.1:g.28839G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1462G= MANE Select ENSP00000262027.5:p.Asp488=
ENST00000262027.9:c.1462G= ENSP00000262027.5:p.Asp488=
ENST00000447721.6:n.1104G=
ENST00000537638.6:c.1462G= ENSP00000446168.2:p.Asp488=
ENST00000545888.6:c.*963G= ENSP00000439307.2:n.*963G=
ENST00000546971.5:n.206G=
ENST00000548630.1:n.23G=
ENST00000548944.1:c.134-4704G= ENSP00000449071.1:n.134-4704G=
ENST00000628866.2:c.*963G= ENSP00000486738.1:n.*963G=
NM_004990.3:c.1462G= NP_004981.2:p.Asp488=
XM_006719398.2:c.760G= XP_006719461.1:p.Asp254=
XM_011538353.1:c.1462G= XP_011536655.1:p.Asp488=
XM_006719398.4:c.760G= XP_006719461.1:p.Asp254=
XR_001748704.2:n.1485G=
XR_002957327.1:n.1409G=
NM_004990.4:c.1462G= MANE Select NP_004981.2:p.Asp488=