Canonical Allele Identifier: CA480395801

Gene: MARS1

Linked Data

• MyVariant Identifiers: chr12:g.57905618A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57511835A>G , CM000674.2:g.57511835A>G	GRCh38
NC_000012.11:g.57905618A>G , CM000674.1:g.57905618A>G	GRCh37
NC_000012.10:g.56191885A>G	NCBI36
NG_034077.1:g.28883A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1506A>G MANE Select	ENSP00000262027.5:p.Gly502=
ENST00000262027.9:c.1506A>G	ENSP00000262027.5:p.Gly502=
ENST00000447721.6:n.1148A>G
ENST00000537638.6:c.1506A>G	ENSP00000446168.2:p.Gly502=
ENST00000545888.6:c.*1007A>G	ENSP00000439307.2:n.*1007A>G
ENST00000546971.5:n.250A>G
ENST00000548630.1:n.67A>G
ENST00000548944.1:c.134-4660A>G	ENSP00000449071.1:n.134-4660A>G
ENST00000549048.1:n.39A>G
ENST00000628866.2:c.*1007A>G	ENSP00000486738.1:n.*1007A>G
NM_004990.3:c.1506A>G	NP_004981.2:p.Gly502=
XM_006719398.2:c.804A>G	XP_006719461.1:p.Gly268=
XM_011538353.1:c.1506A>G	XP_011536655.1:p.Gly502=
XM_006719398.4:c.804A>G	XP_006719461.1:p.Gly268=
XR_001748704.2:n.1529A>G
XR_002957327.1:n.1453A>G
NM_004990.4:c.1506A>G MANE Select	NP_004981.2:p.Gly502=