Canonical Allele Identifier: CA2038898244
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57511510T= , CM000674.2:g.57511510T= GRCh38
NC_000012.11:g.57905293T= , CM000674.1:g.57905293T= GRCh37
NC_000012.10:g.56191560T= NCBI36
NG_034077.1:g.28558T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1369-188T= MANE Select ENSP00000262027.5:n.1369-188T=
ENST00000262027.9:c.1369-188T= ENSP00000262027.5:n.1369-188T=
ENST00000447721.6:n.1011-188T=
ENST00000537638.6:c.1369-188T= ENSP00000446168.2:n.1369-188T=
ENST00000545888.6:c.*870-188T= ENSP00000439307.2:n.*870-188T=
ENST00000548944.1:c.134-4985T= ENSP00000449071.1:n.134-4985T=
ENST00000549603.1:n.315-188T=
ENST00000628866.2:c.*870-188T= ENSP00000486738.1:n.*870-188T=
NM_004990.3:c.1369-188T= NP_004981.2:n.1369-188T=
XM_006719398.2:c.667-188T= XP_006719461.1:n.667-188T=
XM_011538353.1:c.1369-188T= XP_011536655.1:n.1369-188T=
XM_006719398.4:c.667-188T= XP_006719461.1:n.667-188T=
XR_001748704.2:n.1392-188T=
XR_002957327.1:n.1316-188T=
NM_004990.4:c.1369-188T= MANE Select NP_004981.2:n.1369-188T=