Canonical Allele Identifier: CA385461636

Gene: MARS1

Linked Data

• MyVariant Identifiers: chr12:g.57905620C>T (hg19) ; chr12:g.57511837C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57511837C>T , CM000674.2:g.57511837C>T	GRCh38
NC_000012.11:g.57905620C>T , CM000674.1:g.57905620C>T	GRCh37
NC_000012.10:g.56191887C>T	NCBI36
NG_034077.1:g.28885C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1508C>T MANE Select	ENSP00000262027.5:p.Thr503Ile
ENST00000262027.9:c.1508C>T	ENSP00000262027.5:p.Thr503Ile
ENST00000447721.6:n.1150C>T
ENST00000537638.6:c.1508C>T	ENSP00000446168.2:p.Thr503Ile
ENST00000545888.6:c.*1009C>T	ENSP00000439307.2:n.*1009C>T
ENST00000546971.5:n.252C>T
ENST00000548630.1:n.69C>T
ENST00000548944.1:c.134-4658C>T	ENSP00000449071.1:n.134-4658C>T
ENST00000549048.1:n.41C>T
ENST00000628866.2:c.*1009C>T	ENSP00000486738.1:n.*1009C>T
NM_004990.3:c.1508C>T	NP_004981.2:p.Thr503Ile
XM_006719398.2:c.806C>T	XP_006719461.1:p.Thr269Ile
XM_011538353.1:c.1508C>T	XP_011536655.1:p.Thr503Ile
XM_006719398.4:c.806C>T	XP_006719461.1:p.Thr269Ile
XR_001748704.2:n.1531C>T
XR_002957327.1:n.1455C>T
NM_004990.4:c.1508C>T MANE Select	NP_004981.2:p.Thr503Ile