Canonical Allele Identifier: CA2038898414
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57511855_57511856delinsGT , CM000674.2:g.57511855_57511856delinsGT GRCh38
NC_000012.11:g.57905638_57905639delinsGT , CM000674.1:g.57905638_57905639delinsGT GRCh37
NC_000012.10:g.56191905_56191906delinsGT NCBI36
NG_034077.1:g.28903_28904delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1526_1527delinsGT MANE Select ENSP00000262027.5:p.Gly509=
ENST00000262027.9:c.1526_1527delinsGT ENSP00000262027.5:p.Gly509=
ENST00000447721.6:n.1168_1169delinsGT
ENST00000537638.6:c.1526_1527delinsGT ENSP00000446168.2:p.Gly509=
ENST00000545888.6:c.*1027_*1028delinsGT ENSP00000439307.2:n.*1027_*1028delinsGT
ENST00000546971.5:n.270_271delinsGT
ENST00000548630.1:n.87_88delinsGT
ENST00000548944.1:c.134-4640_134-4639delinsGT ENSP00000449071.1:n.134-4640_134-4639delinsGT
ENST00000549048.1:n.59_60delinsGT
ENST00000628866.2:c.*1027_*1028delinsGT ENSP00000486738.1:n.*1027_*1028delinsGT
NM_004990.3:c.1526_1527delinsGT NP_004981.2:p.Gly509=
XM_006719398.2:c.824_825delinsGT XP_006719461.1:p.Gly275=
XM_011538353.1:c.1526_1527delinsGT XP_011536655.1:p.Gly509=
XM_006719398.4:c.824_825delinsGT XP_006719461.1:p.Gly275=
XR_001748704.2:n.1549_1550delinsGT
XR_002957327.1:n.1473_1474delinsGT
NM_004990.4:c.1526_1527delinsGT MANE Select NP_004981.2:p.Gly509=