Canonical Allele Identifier: CA2038898494

Gene: MARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57512044C= , CM000674.2:g.57512044C=	GRCh38
NC_000012.11:g.57905827C= , CM000674.1:g.57905827C=	GRCh37
NC_000012.10:g.56192094C=	NCBI36
NG_034077.1:g.29092C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1576C= MANE Select	ENSP00000262027.5:p.Leu526=
ENST00000262027.9:c.1576C=	ENSP00000262027.5:p.Leu526=
ENST00000447721.6:n.1218C=
ENST00000537638.6:c.1576C=	ENSP00000446168.2:p.Leu526=
ENST00000545888.6:c.*1077C=	ENSP00000439307.2:n.*1077C=
ENST00000546971.5:n.320C=
ENST00000548630.1:n.137C=
ENST00000548944.1:c.134-4451C=	ENSP00000449071.1:n.134-4451C=
ENST00000549048.1:n.109C=
ENST00000628866.2:c.*1077C=	ENSP00000486738.1:n.*1077C=
NM_004990.3:c.1576C=	NP_004981.2:p.Leu526=
XM_006719398.2:c.874C=	XP_006719461.1:p.Leu292=
XM_011538353.1:c.1576C=	XP_011536655.1:p.Leu526=
XM_006719398.4:c.874C=	XP_006719461.1:p.Leu292=
XR_001748704.2:n.1599C=
XR_002957327.1:n.1523C=
NM_004990.4:c.1576C= MANE Select	NP_004981.2:p.Leu526=