Canonical Allele Identifier: CA385463041

Gene: MARS1

Linked Data

• MyVariant Identifiers: chr12:g.57906612G>C (hg19) ; chr12:g.57512829G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57512829G>C , CM000674.2:g.57512829G>C	GRCh38
NC_000012.11:g.57906612G>C , CM000674.1:g.57906612G>C	GRCh37
NC_000012.10:g.56192879G>C	NCBI36
NG_034077.1:g.29877G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1832G>C MANE Select	ENSP00000262027.5:p.Gly611Ala
ENST00000262027.9:c.1832G>C	ENSP00000262027.5:p.Gly611Ala
ENST00000537638.6:c.*124G>C	ENSP00000446168.2:n.*124G>C
ENST00000545888.6:c.*1333G>C	ENSP00000439307.2:n.*1333G>C
ENST00000546971.5:n.576G>C
ENST00000548202.5:n.339G>C
ENST00000548944.1:c.134-3666G>C	ENSP00000449071.1:n.134-3666G>C
ENST00000549048.1:n.497G>C
ENST00000628866.2:c.*1333G>C	ENSP00000486738.1:n.*1333G>C
NM_004990.3:c.1832G>C	NP_004981.2:p.Gly611Ala
XM_006719398.2:c.1130G>C	XP_006719461.1:p.Gly377Ala
XM_011538353.1:c.*124G>C	XP_011536655.1:n.*124G>C
XM_006719398.4:c.1130G>C	XP_006719461.1:p.Gly377Ala
XR_001748704.2:n.1788G>C
XR_002957327.1:n.1779G>C
NM_004990.4:c.1832G>C MANE Select	NP_004981.2:p.Gly611Ala