Canonical Allele Identifier: CA2619465985
Gene: MARS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57512631_57512632del , CM000674.2:g.57512631_57512632del GRCh38
NC_000012.11:g.57906414_57906415del , CM000674.1:g.57906414_57906415del GRCh37
NC_000012.10:g.56192681_56192682del NCBI36
NG_034077.1:g.29679_29680del

Transcript Alleles

HGVS Amino-acid change
ENST00000262027.10:c.1754-120_1754-119del MANE Select ENSP00000262027.5:n.1754-120_1754-119del
ENST00000262027.9:c.1754-120_1754-119del ENSP00000262027.5:n.1754-120_1754-119del
ENST00000537638.6:c.*46-120_*46-119del ENSP00000446168.2:n.*46-120_*46-119del
ENST00000545888.6:c.*1255-120_*1255-119del ENSP00000439307.2:n.*1255-120_*1255-119del
ENST00000546971.5:n.498-120_498-119del
ENST00000548202.5:n.141_142del
ENST00000548944.1:c.134-3864_134-3863del ENSP00000449071.1:n.134-3864_134-3863del
ENST00000549048.1:n.419-120_419-119del
ENST00000628866.2:c.*1255-120_*1255-119del ENSP00000486738.1:n.*1255-120_*1255-119del
NM_004990.3:c.1754-120_1754-119del NP_004981.2:n.1754-120_1754-119del
XM_006719398.2:c.1052-120_1052-119del XP_006719461.1:n.1052-120_1052-119del
XM_011538353.1:c.*46-120_*46-119del XP_011536655.1:n.*46-120_*46-119del
XM_006719398.4:c.1052-120_1052-119del XP_006719461.1:n.1052-120_1052-119del
XR_001748704.2:n.1710-120_1710-119del
XR_002957327.1:n.1701-120_1701-119del
NM_004990.4:c.1754-120_1754-119del MANE Select NP_004981.2:n.1754-120_1754-119del