Canonical Allele Identifier: CA385461911

Gene: MARS1

Linked Data

• MyVariant Identifiers: chr12:g.57905876A>C (hg19) ; chr12:g.57512093A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57512093A>C , CM000674.2:g.57512093A>C	GRCh38
NC_000012.11:g.57905876A>C , CM000674.1:g.57905876A>C	GRCh37
NC_000012.10:g.56192143A>C	NCBI36
NG_034077.1:g.29141A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1625A>C MANE Select	ENSP00000262027.5:p.Asn542Thr
ENST00000262027.9:c.1625A>C	ENSP00000262027.5:p.Asn542Thr
ENST00000447721.6:n.1267A>C
ENST00000537638.6:c.1625A>C	ENSP00000446168.2:p.Asn542Thr
ENST00000545888.6:c.*1126A>C	ENSP00000439307.2:n.*1126A>C
ENST00000546971.5:n.369A>C
ENST00000548630.1:n.186A>C
ENST00000548944.1:c.134-4402A>C	ENSP00000449071.1:n.134-4402A>C
ENST00000549048.1:n.158A>C
ENST00000628866.2:c.*1126A>C	ENSP00000486738.1:n.*1126A>C
NM_004990.3:c.1625A>C	NP_004981.2:p.Asn542Thr
XM_006719398.2:c.923A>C	XP_006719461.1:p.Asn308Thr
XM_011538353.1:c.1625A>C	XP_011536655.1:p.Asn542Thr
XM_006719398.4:c.923A>C	XP_006719461.1:p.Asn308Thr
XR_001748704.2:n.1648A>C
XR_002957327.1:n.1572A>C
NM_004990.4:c.1625A>C MANE Select	NP_004981.2:p.Asn542Thr