Canonical Allele Identifier: CA2038898277
Gene: MARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57511583_57511585delinsCAA , CM000674.2:g.57511583_57511585delinsCAA GRCh38
NC_000012.11:g.57905366_57905368delinsCAA , CM000674.1:g.57905366_57905368delinsCAA GRCh37
NC_000012.10:g.56191633_56191635delinsCAA NCBI36
NG_034077.1:g.28631_28633delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1369-115_1369-113delinsCAA MANE Select ENSP00000262027.5:n.1369-115_1369-113delinsCAA
ENST00000262027.9:c.1369-115_1369-113delinsCAA ENSP00000262027.5:n.1369-115_1369-113delinsCAA
ENST00000447721.6:n.1011-115_1011-113delinsCAA
ENST00000537638.6:c.1369-115_1369-113delinsCAA ENSP00000446168.2:n.1369-115_1369-113delinsCAA
ENST00000545888.6:c.*870-115_*870-113delinsCAA ENSP00000439307.2:n.*870-115_*870-113delinsCAA
ENST00000548944.1:c.134-4912_134-4910delinsCAA ENSP00000449071.1:n.134-4912_134-4910delinsCAA
ENST00000549603.1:n.315-115_315-113delinsCAA
ENST00000628866.2:c.*870-115_*870-113delinsCAA ENSP00000486738.1:n.*870-115_*870-113delinsCAA
NM_004990.3:c.1369-115_1369-113delinsCAA NP_004981.2:n.1369-115_1369-113delinsCAA
XM_006719398.2:c.667-115_667-113delinsCAA XP_006719461.1:n.667-115_667-113delinsCAA
XM_011538353.1:c.1369-115_1369-113delinsCAA XP_011536655.1:n.1369-115_1369-113delinsCAA
XM_006719398.4:c.667-115_667-113delinsCAA XP_006719461.1:n.667-115_667-113delinsCAA
XR_001748704.2:n.1392-115_1392-113delinsCAA
XR_002957327.1:n.1316-115_1316-113delinsCAA
NM_004990.4:c.1369-115_1369-113delinsCAA MANE Select NP_004981.2:n.1369-115_1369-113delinsCAA