Canonical Allele Identifier: CA2038903442
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57512810G= , CM000674.2:g.57512810G= GRCh38
NC_000012.11:g.57906593G= , CM000674.1:g.57906593G= GRCh37
NC_000012.10:g.56192860G= NCBI36
NG_034077.1:g.29858G=

Transcript Alleles

HGVS Amino-acid change
ENST00000262027.10:c.1813G= MANE Select ENSP00000262027.5:p.Asp605=
ENST00000262027.9:c.1813G= ENSP00000262027.5:p.Asp605=
ENST00000537638.6:c.*105G= ENSP00000446168.2:n.*105G=
ENST00000545888.6:c.*1314G= ENSP00000439307.2:n.*1314G=
ENST00000546971.5:n.557G=
ENST00000548202.5:n.320G=
ENST00000548944.1:c.134-3685G= ENSP00000449071.1:n.134-3685G=
ENST00000549048.1:n.478G=
ENST00000628866.2:c.*1314G= ENSP00000486738.1:n.*1314G=
NM_004990.3:c.1813G= NP_004981.2:p.Asp605=
XM_006719398.2:c.1111G= XP_006719461.1:p.Asp371=
XM_011538353.1:c.*105G= XP_011536655.1:n.*105G=
XM_006719398.4:c.1111G= XP_006719461.1:p.Asp371=
XR_001748704.2:n.1769G=
XR_002957327.1:n.1760G=
NM_004990.4:c.1813G= MANE Select NP_004981.2:p.Asp605=