Canonical Allele Identifier: CA480395694

Gene: MARS1

Linked Data

• MyVariant Identifiers: chr12:g.57905517T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57511734T>C , CM000674.2:g.57511734T>C	GRCh38
NC_000012.11:g.57905517T>C , CM000674.1:g.57905517T>C	GRCh37
NC_000012.10:g.56191784T>C	NCBI36
NG_034077.1:g.28782T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1405T>C MANE Select	ENSP00000262027.5:p.Leu469=
ENST00000262027.9:c.1405T>C	ENSP00000262027.5:p.Leu469=
ENST00000447721.6:n.1047T>C
ENST00000537638.6:c.1405T>C	ENSP00000446168.2:p.Leu469=
ENST00000545888.6:c.*906T>C	ENSP00000439307.2:n.*906T>C
ENST00000546971.5:n.149T>C
ENST00000548944.1:c.134-4761T>C	ENSP00000449071.1:n.134-4761T>C
ENST00000549603.1:n.351T>C
ENST00000628866.2:c.*906T>C	ENSP00000486738.1:n.*906T>C
NM_004990.3:c.1405T>C	NP_004981.2:p.Leu469=
XM_006719398.2:c.703T>C	XP_006719461.1:p.Leu235=
XM_011538353.1:c.1405T>C	XP_011536655.1:p.Leu469=
XM_006719398.4:c.703T>C	XP_006719461.1:p.Leu235=
XR_001748704.2:n.1428T>C
XR_002957327.1:n.1352T>C
NM_004990.4:c.1405T>C MANE Select	NP_004981.2:p.Leu469=