Canonical Allele Identifier: CA2038879725
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57489813G= , CM000674.2:g.57489813G= GRCh38
NC_000012.11:g.57883596G= , CM000674.1:g.57883596G= GRCh37
NC_000012.10:g.56169863G= NCBI36
NG_034077.1:g.6861G=
NG_023205.2:g.4002C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.415-83G= MANE Select ENSP00000262027.5:n.415-83G=
ENST00000262027.9:c.415-83G= ENSP00000262027.5:n.415-83G=
ENST00000447721.6:n.133-394G=
ENST00000537638.6:c.415-83G= ENSP00000446168.2:n.415-83G=
ENST00000545888.6:c.414+255G= ENSP00000439307.2:n.414+255G=
ENST00000547501.5:c.*51-83G= ENSP00000447145.1:n.*51-83G=
ENST00000548674.5:n.384+255G=
ENST00000549074.5:c.201-394G= ENSP00000447258.1:n.201-394G=
ENST00000550449.5:n.528-83G=
ENST00000551431.5:c.280-394G= ENSP00000446729.1:n.280-394G=
ENST00000551892.1:c.110-465G= ENSP00000450018.1:n.110-465G=
ENST00000552007.5:c.201-83G= ENSP00000448576.1:n.201-83G=
ENST00000552371.1:c.30-83G=
ENST00000553123.1:n.639-83G=
ENST00000553162.5:n.438-83G=
ENST00000628866.2:c.280-394G= ENSP00000486738.1:n.280-394G=
ENST00000630571.2:c.201-83G= ENSP00000485951.1:n.201-83G=
ENST00000630803.1:c.110-465G= ENSP00000486356.1:n.110-465G=
NM_004990.3:c.415-83G= NP_004981.2:n.415-83G=
XM_006719398.2:c.-213+255G= XP_006719461.1:n.-213+255G=
XM_011538353.1:c.415-83G= XP_011536655.1:n.415-83G=
XM_006719398.4:c.-213+255G= XP_006719461.1:n.-213+255G=
XR_001748704.2:n.438-83G=
XR_002957327.1:n.437+255G=
NM_004990.4:c.415-83G= MANE Select NP_004981.2:n.415-83G=