Canonical Allele Identifier: CA385461617

Gene: MARS1

Linked Data

• MyVariant Identifiers: chr12:g.57905613T>A (hg19) ; chr12:g.57511830T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57511830T>A , CM000674.2:g.57511830T>A	GRCh38
NC_000012.11:g.57905613T>A , CM000674.1:g.57905613T>A	GRCh37
NC_000012.10:g.56191880T>A	NCBI36
NG_034077.1:g.28878T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1501T>A MANE Select	ENSP00000262027.5:p.Trp501Arg
ENST00000262027.9:c.1501T>A	ENSP00000262027.5:p.Trp501Arg
ENST00000447721.6:n.1143T>A
ENST00000537638.6:c.1501T>A	ENSP00000446168.2:p.Trp501Arg
ENST00000545888.6:c.*1002T>A	ENSP00000439307.2:n.*1002T>A
ENST00000546971.5:n.245T>A
ENST00000548630.1:n.62T>A
ENST00000548944.1:c.134-4665T>A	ENSP00000449071.1:n.134-4665T>A
ENST00000549048.1:n.34T>A
ENST00000628866.2:c.*1002T>A	ENSP00000486738.1:n.*1002T>A
NM_004990.3:c.1501T>A	NP_004981.2:p.Trp501Arg
XM_006719398.2:c.799T>A	XP_006719461.1:p.Trp267Arg
XM_011538353.1:c.1501T>A	XP_011536655.1:p.Trp501Arg
XM_006719398.4:c.799T>A	XP_006719461.1:p.Trp267Arg
XR_001748704.2:n.1524T>A
XR_002957327.1:n.1448T>A
NM_004990.4:c.1501T>A MANE Select	NP_004981.2:p.Trp501Arg