Canonical Allele Identifier: CA2038903181
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57512627A= , CM000674.2:g.57512627A= GRCh38
NC_000012.11:g.57906410A= , CM000674.1:g.57906410A= GRCh37
NC_000012.10:g.56192677A= NCBI36
NG_034077.1:g.29675A=

Transcript Alleles

HGVS Amino-acid change
ENST00000262027.10:c.1754-124A= MANE Select ENSP00000262027.5:n.1754-124A=
ENST00000262027.9:c.1754-124A= ENSP00000262027.5:n.1754-124A=
ENST00000537638.6:c.*46-124A= ENSP00000446168.2:n.*46-124A=
ENST00000545888.6:c.*1255-124A= ENSP00000439307.2:n.*1255-124A=
ENST00000546971.5:n.498-124A=
ENST00000548202.5:n.137A=
ENST00000548944.1:c.134-3868A= ENSP00000449071.1:n.134-3868A=
ENST00000549048.1:n.419-124A=
ENST00000628866.2:c.*1255-124A= ENSP00000486738.1:n.*1255-124A=
NM_004990.3:c.1754-124A= NP_004981.2:n.1754-124A=
XM_006719398.2:c.1052-124A= XP_006719461.1:n.1052-124A=
XM_011538353.1:c.*46-124A= XP_011536655.1:n.*46-124A=
XM_006719398.4:c.1052-124A= XP_006719461.1:n.1052-124A=
XR_001748704.2:n.1710-124A=
XR_002957327.1:n.1701-124A=
NM_004990.4:c.1754-124A= MANE Select NP_004981.2:n.1754-124A=