Canonical Allele Identifier: CA2038903465
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57512820A= , CM000674.2:g.57512820A= GRCh38
NC_000012.11:g.57906603A= , CM000674.1:g.57906603A= GRCh37
NC_000012.10:g.56192870A= NCBI36
NG_034077.1:g.29868A=

Transcript Alleles

HGVS Amino-acid change
ENST00000262027.10:c.1823A= MANE Select ENSP00000262027.5:p.Gln608=
ENST00000262027.9:c.1823A= ENSP00000262027.5:p.Gln608=
ENST00000537638.6:c.*115A= ENSP00000446168.2:n.*115A=
ENST00000545888.6:c.*1324A= ENSP00000439307.2:n.*1324A=
ENST00000546971.5:n.567A=
ENST00000548202.5:n.330A=
ENST00000548944.1:c.134-3675A= ENSP00000449071.1:n.134-3675A=
ENST00000549048.1:n.488A=
ENST00000628866.2:c.*1324A= ENSP00000486738.1:n.*1324A=
NM_004990.3:c.1823A= NP_004981.2:p.Gln608=
XM_006719398.2:c.1121A= XP_006719461.1:p.Gln374=
XM_011538353.1:c.*115A= XP_011536655.1:n.*115A=
XM_006719398.4:c.1121A= XP_006719461.1:p.Gln374=
XR_001748704.2:n.1779A=
XR_002957327.1:n.1770A=
NM_004990.4:c.1823A= MANE Select NP_004981.2:p.Gln608=