Canonical Allele Identifier: CA2038898251
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57511529A= , CM000674.2:g.57511529A= GRCh38
NC_000012.11:g.57905312A= , CM000674.1:g.57905312A= GRCh37
NC_000012.10:g.56191579A= NCBI36
NG_034077.1:g.28577A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1369-169A= MANE Select ENSP00000262027.5:n.1369-169A=
ENST00000262027.9:c.1369-169A= ENSP00000262027.5:n.1369-169A=
ENST00000447721.6:n.1011-169A=
ENST00000537638.6:c.1369-169A= ENSP00000446168.2:n.1369-169A=
ENST00000545888.6:c.*870-169A= ENSP00000439307.2:n.*870-169A=
ENST00000548944.1:c.134-4966A= ENSP00000449071.1:n.134-4966A=
ENST00000549603.1:n.315-169A=
ENST00000628866.2:c.*870-169A= ENSP00000486738.1:n.*870-169A=
NM_004990.3:c.1369-169A= NP_004981.2:n.1369-169A=
XM_006719398.2:c.667-169A= XP_006719461.1:n.667-169A=
XM_011538353.1:c.1369-169A= XP_011536655.1:n.1369-169A=
XM_006719398.4:c.667-169A= XP_006719461.1:n.667-169A=
XR_001748704.2:n.1392-169A=
XR_002957327.1:n.1316-169A=
NM_004990.4:c.1369-169A= MANE Select NP_004981.2:n.1369-169A=