Canonical Allele Identifier: CA385461892

Gene: MARS1

Linked Data

• MyVariant Identifiers: chr12:g.57905869T>A (hg19) ; chr12:g.57512086T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57512086T>A , CM000674.2:g.57512086T>A	GRCh38
NC_000012.11:g.57905869T>A , CM000674.1:g.57905869T>A	GRCh37
NC_000012.10:g.56192136T>A	NCBI36
NG_034077.1:g.29134T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1618T>A MANE Select	ENSP00000262027.5:p.Trp540Arg
ENST00000262027.9:c.1618T>A	ENSP00000262027.5:p.Trp540Arg
ENST00000447721.6:n.1260T>A
ENST00000537638.6:c.1618T>A	ENSP00000446168.2:p.Trp540Arg
ENST00000545888.6:c.*1119T>A	ENSP00000439307.2:n.*1119T>A
ENST00000546971.5:n.362T>A
ENST00000548630.1:n.179T>A
ENST00000548944.1:c.134-4409T>A	ENSP00000449071.1:n.134-4409T>A
ENST00000549048.1:n.151T>A
ENST00000628866.2:c.*1119T>A	ENSP00000486738.1:n.*1119T>A
NM_004990.3:c.1618T>A	NP_004981.2:p.Trp540Arg
XM_006719398.2:c.916T>A	XP_006719461.1:p.Trp306Arg
XM_011538353.1:c.1618T>A	XP_011536655.1:p.Trp540Arg
XM_006719398.4:c.916T>A	XP_006719461.1:p.Trp306Arg
XR_001748704.2:n.1641T>A
XR_002957327.1:n.1565T>A
NM_004990.4:c.1618T>A MANE Select	NP_004981.2:p.Trp540Arg