Canonical Allele Identifier: CA2038903195

Gene: MARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57512634_57512637delinsATGT , CM000674.2:g.57512634_57512637delinsATGT	GRCh38
NC_000012.11:g.57906417_57906420delinsATGT , CM000674.1:g.57906417_57906420delinsATGT	GRCh37
NC_000012.10:g.56192684_56192687delinsATGT	NCBI36
NG_034077.1:g.29682_29685delinsATGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000262027.10:c.1754-117_1754-114delinsATGT MANE Select	ENSP00000262027.5:n.1754-117_1754-114delinsATGT
ENST00000262027.9:c.1754-117_1754-114delinsATGT	ENSP00000262027.5:n.1754-117_1754-114delinsATGT
ENST00000537638.6:c.*46-117_*46-114delinsATGT	ENSP00000446168.2:n.*46-117_*46-114delinsATGT
ENST00000545888.6:c.*1255-117_*1255-114delinsATGT	ENSP00000439307.2:n.*1255-117_*1255-114delinsATGT
ENST00000546971.5:n.498-117_498-114delinsATGT
ENST00000548202.5:n.144_147delinsATGT
ENST00000548944.1:c.134-3861_134-3858delinsATGT	ENSP00000449071.1:n.134-3861_134-3858delinsATGT
ENST00000549048.1:n.419-117_419-114delinsATGT
ENST00000628866.2:c.*1255-117_*1255-114delinsATGT	ENSP00000486738.1:n.*1255-117_*1255-114delinsATGT
NM_004990.3:c.1754-117_1754-114delinsATGT	NP_004981.2:n.1754-117_1754-114delinsATGT
XM_006719398.2:c.1052-117_1052-114delinsATGT	XP_006719461.1:n.1052-117_1052-114delinsATGT
XM_011538353.1:c.*46-117_*46-114delinsATGT	XP_011536655.1:n.*46-117_*46-114delinsATGT
XM_006719398.4:c.1052-117_1052-114delinsATGT	XP_006719461.1:n.1052-117_1052-114delinsATGT
XR_001748704.2:n.1710-117_1710-114delinsATGT
XR_002957327.1:n.1701-117_1701-114delinsATGT
NM_004990.4:c.1754-117_1754-114delinsATGT MANE Select	NP_004981.2:n.1754-117_1754-114delinsATGT