Canonical Allele Identifier: CA2038898493
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57512042A= , CM000674.2:g.57512042A= GRCh38
NC_000012.11:g.57905825A= , CM000674.1:g.57905825A= GRCh37
NC_000012.10:g.56192092A= NCBI36
NG_034077.1:g.29090A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1574A= MANE Select ENSP00000262027.5:p.Tyr525=
ENST00000262027.9:c.1574A= ENSP00000262027.5:p.Tyr525=
ENST00000447721.6:n.1216A=
ENST00000537638.6:c.1574A= ENSP00000446168.2:p.Tyr525=
ENST00000545888.6:c.*1075A= ENSP00000439307.2:n.*1075A=
ENST00000546971.5:n.318A=
ENST00000548630.1:n.135A=
ENST00000548944.1:c.134-4453A= ENSP00000449071.1:n.134-4453A=
ENST00000549048.1:n.107A=
ENST00000628866.2:c.*1075A= ENSP00000486738.1:n.*1075A=
NM_004990.3:c.1574A= NP_004981.2:p.Tyr525=
XM_006719398.2:c.872A= XP_006719461.1:p.Tyr291=
XM_011538353.1:c.1574A= XP_011536655.1:p.Tyr525=
XM_006719398.4:c.872A= XP_006719461.1:p.Tyr291=
XR_001748704.2:n.1597A=
XR_002957327.1:n.1521A=
NM_004990.4:c.1574A= MANE Select NP_004981.2:p.Tyr525=