Canonical Allele Identifier: CA2038903474
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57512826C= , CM000674.2:g.57512826C= GRCh38
NC_000012.11:g.57906609C= , CM000674.1:g.57906609C= GRCh37
NC_000012.10:g.56192876C= NCBI36
NG_034077.1:g.29874C=

Transcript Alleles

HGVS Amino-acid change
ENST00000262027.10:c.1829C= MANE Select ENSP00000262027.5:p.Thr610=
ENST00000262027.9:c.1829C= ENSP00000262027.5:p.Thr610=
ENST00000537638.6:c.*121C= ENSP00000446168.2:n.*121C=
ENST00000545888.6:c.*1330C= ENSP00000439307.2:n.*1330C=
ENST00000546971.5:n.573C=
ENST00000548202.5:n.336C=
ENST00000548944.1:c.134-3669C= ENSP00000449071.1:n.134-3669C=
ENST00000549048.1:n.494C=
ENST00000628866.2:c.*1330C= ENSP00000486738.1:n.*1330C=
NM_004990.3:c.1829C= NP_004981.2:p.Thr610=
XM_006719398.2:c.1127C= XP_006719461.1:p.Thr376=
XM_011538353.1:c.*121C= XP_011536655.1:n.*121C=
XM_006719398.4:c.1127C= XP_006719461.1:p.Thr376=
XR_001748704.2:n.1785C=
XR_002957327.1:n.1776C=
NM_004990.4:c.1829C= MANE Select NP_004981.2:p.Thr610=