Canonical Allele Identifier: CA2038898501

Gene: MARS1

Linked Data

• dbSNP Id: rs1877548280

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57512068dup , CM000674.2:g.57512068dup	GRCh38
NC_000012.11:g.57905851dup , CM000674.1:g.57905851dup	GRCh37
NC_000012.10:g.56192118dup	NCBI36
NG_034077.1:g.29116dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1600dup MANE Select	ENSP00000262027.5:p.Asp534GlyfsTer28
ENST00000262027.9:c.1600dup	ENSP00000262027.5:p.Asp534GlyfsTer28
ENST00000447721.6:n.1242dup
ENST00000537638.6:c.1600dup	ENSP00000446168.2:p.Asp534GlyfsTer?
ENST00000545888.6:c.*1101dup	ENSP00000439307.2:n.*1101dup
ENST00000546971.5:n.344dup
ENST00000548630.1:n.161dup
ENST00000548944.1:c.134-4427dup	ENSP00000449071.1:n.134-4427dup
ENST00000549048.1:n.133dup
ENST00000628866.2:c.*1101dup	ENSP00000486738.1:n.*1101dup
NM_004990.3:c.1600dup	NP_004981.2:p.Asp534GlyfsTer28
XM_006719398.2:c.898dup	XP_006719461.1:p.Asp300GlyfsTer28
XM_011538353.1:c.1600dup	XP_011536655.1:p.Asp534GlyfsTer?
XM_006719398.4:c.898dup	XP_006719461.1:p.Asp300GlyfsTer28
XR_001748704.2:n.1623dup
XR_002957327.1:n.1547dup
NM_004990.4:c.1600dup MANE Select	NP_004981.2:p.Asp534GlyfsTer28