Canonical Allele Identifier: CA2038898484
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57512010A= , CM000674.2:g.57512010A= GRCh38
NC_000012.11:g.57905793A= , CM000674.1:g.57905793A= GRCh37
NC_000012.10:g.56192060A= NCBI36
NG_034077.1:g.29058A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1542A= MANE Select ENSP00000262027.5:p.Val514=
ENST00000262027.9:c.1542A= ENSP00000262027.5:p.Val514=
ENST00000447721.6:n.1184A=
ENST00000537638.6:c.1542A= ENSP00000446168.2:p.Val514=
ENST00000545888.6:c.*1043A= ENSP00000439307.2:n.*1043A=
ENST00000546971.5:n.286A=
ENST00000548630.1:n.103A=
ENST00000548944.1:c.134-4485A= ENSP00000449071.1:n.134-4485A=
ENST00000549048.1:n.75A=
ENST00000628866.2:c.*1043A= ENSP00000486738.1:n.*1043A=
NM_004990.3:c.1542A= NP_004981.2:p.Val514=
XM_006719398.2:c.840A= XP_006719461.1:p.Val280=
XM_011538353.1:c.1542A= XP_011536655.1:p.Val514=
XM_006719398.4:c.840A= XP_006719461.1:p.Val280=
XR_001748704.2:n.1565A=
XR_002957327.1:n.1489A=
NM_004990.4:c.1542A= MANE Select NP_004981.2:p.Val514=