Canonical Allele Identifier: CA2038898243
Gene: MARS1 HGNC NCBI

Linked Data

dbSNP Id: rs1594832206

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57511508T>G , CM000674.2:g.57511508T>G GRCh38
NC_000012.11:g.57905291T>G , CM000674.1:g.57905291T>G GRCh37
NC_000012.10:g.56191558T>G NCBI36
NG_034077.1:g.28556T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262027.10:c.1369-190T>G MANE Select ENSP00000262027.5:n.1369-190T>G
ENST00000262027.9:c.1369-190T>G ENSP00000262027.5:n.1369-190T>G
ENST00000447721.6:n.1011-190T>G
ENST00000537638.6:c.1369-190T>G ENSP00000446168.2:n.1369-190T>G
ENST00000545888.6:c.*870-190T>G ENSP00000439307.2:n.*870-190T>G
ENST00000548944.1:c.134-4987T>G ENSP00000449071.1:n.134-4987T>G
ENST00000549603.1:n.315-190T>G
ENST00000628866.2:c.*870-190T>G ENSP00000486738.1:n.*870-190T>G
NM_004990.3:c.1369-190T>G NP_004981.2:n.1369-190T>G
XM_006719398.2:c.667-190T>G XP_006719461.1:n.667-190T>G
XM_011538353.1:c.1369-190T>G XP_011536655.1:n.1369-190T>G
XM_006719398.4:c.667-190T>G XP_006719461.1:n.667-190T>G
XR_001748704.2:n.1392-190T>G
XR_002957327.1:n.1316-190T>G
NM_004990.4:c.1369-190T>G MANE Select NP_004981.2:n.1369-190T>G