Canonical Allele Identifier: CA480395813

Gene: MARS1

Linked Data

• MyVariant Identifiers: chr12:g.57905630C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57511847C>T , CM000674.2:g.57511847C>T	GRCh38
NC_000012.11:g.57905630C>T , CM000674.1:g.57905630C>T	GRCh37
NC_000012.10:g.56191897C>T	NCBI36
NG_034077.1:g.28895C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1518C>T MANE Select	ENSP00000262027.5:p.Pro506=
ENST00000262027.9:c.1518C>T	ENSP00000262027.5:p.Pro506=
ENST00000447721.6:n.1160C>T
ENST00000537638.6:c.1518C>T	ENSP00000446168.2:p.Pro506=
ENST00000545888.6:c.*1019C>T	ENSP00000439307.2:n.*1019C>T
ENST00000546971.5:n.262C>T
ENST00000548630.1:n.79C>T
ENST00000548944.1:c.134-4648C>T	ENSP00000449071.1:n.134-4648C>T
ENST00000549048.1:n.51C>T
ENST00000628866.2:c.*1019C>T	ENSP00000486738.1:n.*1019C>T
NM_004990.3:c.1518C>T	NP_004981.2:p.Pro506=
XM_006719398.2:c.816C>T	XP_006719461.1:p.Pro272=
XM_011538353.1:c.1518C>T	XP_011536655.1:p.Pro506=
XM_006719398.4:c.816C>T	XP_006719461.1:p.Pro272=
XR_001748704.2:n.1541C>T
XR_002957327.1:n.1465C>T
NM_004990.4:c.1518C>T MANE Select	NP_004981.2:p.Pro506=