Canonical Allele Identifier: CA2038898266
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57511555T= , CM000674.2:g.57511555T= GRCh38
NC_000012.11:g.57905338T= , CM000674.1:g.57905338T= GRCh37
NC_000012.10:g.56191605T= NCBI36
NG_034077.1:g.28603T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1369-143T= MANE Select ENSP00000262027.5:n.1369-143T=
ENST00000262027.9:c.1369-143T= ENSP00000262027.5:n.1369-143T=
ENST00000447721.6:n.1011-143T=
ENST00000537638.6:c.1369-143T= ENSP00000446168.2:n.1369-143T=
ENST00000545888.6:c.*870-143T= ENSP00000439307.2:n.*870-143T=
ENST00000548944.1:c.134-4940T= ENSP00000449071.1:n.134-4940T=
ENST00000549603.1:n.315-143T=
ENST00000628866.2:c.*870-143T= ENSP00000486738.1:n.*870-143T=
NM_004990.3:c.1369-143T= NP_004981.2:n.1369-143T=
XM_006719398.2:c.667-143T= XP_006719461.1:n.667-143T=
XM_011538353.1:c.1369-143T= XP_011536655.1:n.1369-143T=
XM_006719398.4:c.667-143T= XP_006719461.1:n.667-143T=
XR_001748704.2:n.1392-143T=
XR_002957327.1:n.1316-143T=
NM_004990.4:c.1369-143T= MANE Select NP_004981.2:n.1369-143T=