Canonical Allele Identifier: CA2038898479

Gene: MARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57511998T= , CM000674.2:g.57511998T=	GRCh38
NC_000012.11:g.57905781T= , CM000674.1:g.57905781T=	GRCh37
NC_000012.10:g.56192048T=	NCBI36
NG_034077.1:g.29046T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1540-10T= MANE Select	ENSP00000262027.5:n.1540-10T=
ENST00000262027.9:c.1540-10T=	ENSP00000262027.5:n.1540-10T=
ENST00000447721.6:n.1182-10T=
ENST00000537638.6:c.1540-10T=	ENSP00000446168.2:n.1540-10T=
ENST00000545888.6:c.*1041-10T=	ENSP00000439307.2:n.*1041-10T=
ENST00000546971.5:n.284-10T=
ENST00000548630.1:n.101-10T=
ENST00000548944.1:c.134-4497T=	ENSP00000449071.1:n.134-4497T=
ENST00000549048.1:n.73-10T=
ENST00000628866.2:c.*1041-10T=	ENSP00000486738.1:n.*1041-10T=
NM_004990.3:c.1540-10T=	NP_004981.2:n.1540-10T=
XM_006719398.2:c.838-10T=	XP_006719461.1:n.838-10T=
XM_011538353.1:c.1540-10T=	XP_011536655.1:n.1540-10T=
XM_006719398.4:c.838-10T=	XP_006719461.1:n.838-10T=
XR_001748704.2:n.1563-10T=
XR_002957327.1:n.1487-10T=
NM_004990.4:c.1540-10T= MANE Select	NP_004981.2:n.1540-10T=