Canonical Allele Identifier: CA2038898401
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57511828A= , CM000674.2:g.57511828A= GRCh38
NC_000012.11:g.57905611A= , CM000674.1:g.57905611A= GRCh37
NC_000012.10:g.56191878A= NCBI36
NG_034077.1:g.28876A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1499A= MANE Select ENSP00000262027.5:p.Lys500=
ENST00000262027.9:c.1499A= ENSP00000262027.5:p.Lys500=
ENST00000447721.6:n.1141A=
ENST00000537638.6:c.1499A= ENSP00000446168.2:p.Lys500=
ENST00000545888.6:c.*1000A= ENSP00000439307.2:n.*1000A=
ENST00000546971.5:n.243A=
ENST00000548630.1:n.60A=
ENST00000548944.1:c.134-4667A= ENSP00000449071.1:n.134-4667A=
ENST00000549048.1:n.32A=
ENST00000628866.2:c.*1000A= ENSP00000486738.1:n.*1000A=
NM_004990.3:c.1499A= NP_004981.2:p.Lys500=
XM_006719398.2:c.797A= XP_006719461.1:p.Lys266=
XM_011538353.1:c.1499A= XP_011536655.1:p.Lys500=
XM_006719398.4:c.797A= XP_006719461.1:p.Lys266=
XR_001748704.2:n.1522A=
XR_002957327.1:n.1446A=
NM_004990.4:c.1499A= MANE Select NP_004981.2:p.Lys500=