Canonical Allele Identifier: CA2038898465

Gene: MARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57511966T= , CM000674.2:g.57511966T=	GRCh38
NC_000012.11:g.57905749T= , CM000674.1:g.57905749T=	GRCh37
NC_000012.10:g.56192016T=	NCBI36
NG_034077.1:g.29014T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1540-42T= MANE Select	ENSP00000262027.5:n.1540-42T=
ENST00000262027.9:c.1540-42T=	ENSP00000262027.5:n.1540-42T=
ENST00000447721.6:n.1182-42T=
ENST00000537638.6:c.1540-42T=	ENSP00000446168.2:n.1540-42T=
ENST00000545888.6:c.*1041-42T=	ENSP00000439307.2:n.*1041-42T=
ENST00000546971.5:n.284-42T=
ENST00000548630.1:n.101-42T=
ENST00000548944.1:c.134-4529T=	ENSP00000449071.1:n.134-4529T=
ENST00000549048.1:n.73-42T=
ENST00000628866.2:c.*1041-42T=	ENSP00000486738.1:n.*1041-42T=
NM_004990.3:c.1540-42T=	NP_004981.2:n.1540-42T=
XM_006719398.2:c.838-42T=	XP_006719461.1:n.838-42T=
XM_011538353.1:c.1540-42T=	XP_011536655.1:n.1540-42T=
XM_006719398.4:c.838-42T=	XP_006719461.1:n.838-42T=
XR_001748704.2:n.1563-42T=
XR_002957327.1:n.1487-42T=
NM_004990.4:c.1540-42T= MANE Select	NP_004981.2:n.1540-42T=