Canonical Allele Identifier: CA2038898291

Gene: MARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57511600A= , CM000674.2:g.57511600A=	GRCh38
NC_000012.11:g.57905383A= , CM000674.1:g.57905383A=	GRCh37
NC_000012.10:g.56191650A=	NCBI36
NG_034077.1:g.28648A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1369-98A= MANE Select	ENSP00000262027.5:n.1369-98A=
ENST00000262027.9:c.1369-98A=	ENSP00000262027.5:n.1369-98A=
ENST00000447721.6:n.1011-98A=
ENST00000537638.6:c.1369-98A=	ENSP00000446168.2:n.1369-98A=
ENST00000545888.6:c.*870-98A=	ENSP00000439307.2:n.*870-98A=
ENST00000546971.5:n.15A=
ENST00000548944.1:c.134-4895A=	ENSP00000449071.1:n.134-4895A=
ENST00000549603.1:n.315-98A=
ENST00000628866.2:c.*870-98A=	ENSP00000486738.1:n.*870-98A=
NM_004990.3:c.1369-98A=	NP_004981.2:n.1369-98A=
XM_006719398.2:c.667-98A=	XP_006719461.1:n.667-98A=
XM_011538353.1:c.1369-98A=	XP_011536655.1:n.1369-98A=
XM_006719398.4:c.667-98A=	XP_006719461.1:n.667-98A=
XR_001748704.2:n.1392-98A=
XR_002957327.1:n.1316-98A=
NM_004990.4:c.1369-98A= MANE Select	NP_004981.2:n.1369-98A=