Canonical Allele Identifier: CA2038879851

Gene: MARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57489887C= , CM000674.2:g.57489887C=	GRCh38
NC_000012.11:g.57883670C= , CM000674.1:g.57883670C=	GRCh37
NC_000012.10:g.56169937C=	NCBI36
NG_034077.1:g.6935C=
NG_023205.2:g.3928G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262027.10:c.415-9C= MANE Select	ENSP00000262027.5:n.415-9C=
ENST00000262027.9:c.415-9C=	ENSP00000262027.5:n.415-9C=
ENST00000447721.6:n.133-320C=
ENST00000537638.6:c.415-9C=	ENSP00000446168.2:n.415-9C=
ENST00000545888.6:c.415-320C=	ENSP00000439307.2:n.415-320C=
ENST00000547501.5:c.*51-9C=	ENSP00000447145.1:n.*51-9C=
ENST00000548674.5:n.385-320C=
ENST00000549074.5:c.201-320C=	ENSP00000447258.1:n.201-320C=
ENST00000550449.5:n.528-9C=
ENST00000551431.5:c.280-320C=	ENSP00000446729.1:n.280-320C=
ENST00000551892.1:c.110-391C=	ENSP00000450018.1:n.110-391C=
ENST00000552007.5:c.201-9C=	ENSP00000448576.1:n.201-9C=
ENST00000552371.1:c.30-9C=
ENST00000553123.1:n.639-9C=
ENST00000553162.5:n.438-9C=
ENST00000628866.2:c.280-320C=	ENSP00000486738.1:n.280-320C=
ENST00000630571.2:c.201-9C=	ENSP00000485951.1:n.201-9C=
ENST00000630803.1:c.110-391C=	ENSP00000486356.1:n.110-391C=
NM_004990.3:c.415-9C=	NP_004981.2:n.415-9C=
XM_006719398.2:c.-212-320C=	XP_006719461.1:n.-212-320C=
XM_011538353.1:c.415-9C=	XP_011536655.1:n.415-9C=
XM_006719398.4:c.-212-320C=	XP_006719461.1:n.-212-320C=
XR_001748704.2:n.438-9C=
XR_002957327.1:n.438-320C=
NM_004990.4:c.415-9C= MANE Select	NP_004981.2:n.415-9C=