Canonical Allele Identifier: CA2038898491
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57512036T= , CM000674.2:g.57512036T= GRCh38
NC_000012.11:g.57905819T= , CM000674.1:g.57905819T= GRCh37
NC_000012.10:g.56192086T= NCBI36
NG_034077.1:g.29084T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1568T= MANE Select ENSP00000262027.5:p.Ile523=
ENST00000262027.9:c.1568T= ENSP00000262027.5:p.Ile523=
ENST00000447721.6:n.1210T=
ENST00000537638.6:c.1568T= ENSP00000446168.2:p.Ile523=
ENST00000545888.6:c.*1069T= ENSP00000439307.2:n.*1069T=
ENST00000546971.5:n.312T=
ENST00000548630.1:n.129T=
ENST00000548944.1:c.134-4459T= ENSP00000449071.1:n.134-4459T=
ENST00000549048.1:n.101T=
ENST00000628866.2:c.*1069T= ENSP00000486738.1:n.*1069T=
NM_004990.3:c.1568T= NP_004981.2:p.Ile523=
XM_006719398.2:c.866T= XP_006719461.1:p.Ile289=
XM_011538353.1:c.1568T= XP_011536655.1:p.Ile523=
XM_006719398.4:c.866T= XP_006719461.1:p.Ile289=
XR_001748704.2:n.1591T=
XR_002957327.1:n.1515T=
NM_004990.4:c.1568T= MANE Select NP_004981.2:p.Ile523=