Canonical Allele Identifier: CA2038898230
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57511482_57511485delinsTAGG , CM000674.2:g.57511482_57511485delinsTAGG GRCh38
NC_000012.11:g.57905265_57905268delinsTAGG , CM000674.1:g.57905265_57905268delinsTAGG GRCh37
NC_000012.10:g.56191532_56191535delinsTAGG NCBI36
NG_034077.1:g.28530_28533delinsTAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1369-216_1369-213delinsTAGG MANE Select ENSP00000262027.5:n.1369-216_1369-213delinsTAGG
ENST00000262027.9:c.1369-216_1369-213delinsTAGG ENSP00000262027.5:n.1369-216_1369-213delinsTAGG
ENST00000447721.6:n.1011-216_1011-213delinsTAGG
ENST00000537638.6:c.1369-216_1369-213delinsTAGG ENSP00000446168.2:n.1369-216_1369-213delinsTAGG
ENST00000545888.6:c.*870-216_*870-213delinsTAGG ENSP00000439307.2:n.*870-216_*870-213delinsTAGG
ENST00000548944.1:c.134-5013_134-5010delinsTAGG ENSP00000449071.1:n.134-5013_134-5010delinsTAGG
ENST00000549603.1:n.315-216_315-213delinsTAGG
ENST00000628866.2:c.*870-216_*870-213delinsTAGG ENSP00000486738.1:n.*870-216_*870-213delinsTAGG
NM_004990.3:c.1369-216_1369-213delinsTAGG NP_004981.2:n.1369-216_1369-213delinsTAGG
XM_006719398.2:c.667-216_667-213delinsTAGG XP_006719461.1:n.667-216_667-213delinsTAGG
XM_011538353.1:c.1369-216_1369-213delinsTAGG XP_011536655.1:n.1369-216_1369-213delinsTAGG
XM_006719398.4:c.667-216_667-213delinsTAGG XP_006719461.1:n.667-216_667-213delinsTAGG
XR_001748704.2:n.1392-216_1392-213delinsTAGG
XR_002957327.1:n.1316-216_1316-213delinsTAGG
NM_004990.4:c.1369-216_1369-213delinsTAGG MANE Select NP_004981.2:n.1369-216_1369-213delinsTAGG