Canonical Allele Identifier: CA2038879676

Gene: MARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57489764T= , CM000674.2:g.57489764T=	GRCh38
NC_000012.11:g.57883547T= , CM000674.1:g.57883547T=	GRCh37
NC_000012.10:g.56169814T=	NCBI36
NG_034077.1:g.6812T=
NG_023205.2:g.4051A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.415-132T= MANE Select	ENSP00000262027.5:n.415-132T=
ENST00000262027.9:c.415-132T=	ENSP00000262027.5:n.415-132T=
ENST00000447721.6:n.133-443T=
ENST00000537638.6:c.415-132T=	ENSP00000446168.2:n.415-132T=
ENST00000545888.6:c.414+206T=	ENSP00000439307.2:n.414+206T=
ENST00000547501.5:c.*51-132T=	ENSP00000447145.1:n.*51-132T=
ENST00000548674.5:n.384+206T=
ENST00000549074.5:c.201-443T=	ENSP00000447258.1:n.201-443T=
ENST00000550449.5:n.528-132T=
ENST00000551431.5:c.279+419T=	ENSP00000446729.1:n.279+419T=
ENST00000551842.5:n.643T=
ENST00000551892.1:c.110-514T=	ENSP00000450018.1:n.110-514T=
ENST00000552007.5:c.201-132T=	ENSP00000448576.1:n.201-132T=
ENST00000552371.1:c.30-132T=
ENST00000553123.1:n.639-132T=
ENST00000553162.5:n.438-132T=
ENST00000628866.2:c.279+419T=	ENSP00000486738.1:n.279+419T=
ENST00000630571.2:c.201-132T=	ENSP00000485951.1:n.201-132T=
ENST00000630803.1:c.110-514T=	ENSP00000486356.1:n.110-514T=
NM_004990.3:c.415-132T=	NP_004981.2:n.415-132T=
XM_006719398.2:c.-213+206T=	XP_006719461.1:n.-213+206T=
XM_011538353.1:c.415-132T=	XP_011536655.1:n.415-132T=
XM_006719398.4:c.-213+206T=	XP_006719461.1:n.-213+206T=
XR_001748704.2:n.438-132T=
XR_002957327.1:n.437+206T=
NM_004990.4:c.415-132T= MANE Select	NP_004981.2:n.415-132T=