Canonical Allele Identifier: CA2619465973

Gene: MARS1

Linked Data

• gnomAD v4: 12-57512612-C-CAT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57512614_57512615dup , CM000674.2:g.57512614_57512615dup	GRCh38
NC_000012.11:g.57906397_57906398dup , CM000674.1:g.57906397_57906398dup	GRCh37
NC_000012.10:g.56192664_56192665dup	NCBI36
NG_034077.1:g.29662_29663dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000262027.10:c.1754-137_1754-136dup MANE Select	ENSP00000262027.5:n.1754-137_1754-136dup
ENST00000262027.9:c.1754-137_1754-136dup	ENSP00000262027.5:n.1754-137_1754-136dup
ENST00000537638.6:c.*46-137_*46-136dup	ENSP00000446168.2:n.*46-137_*46-136dup
ENST00000545888.6:c.*1255-137_*1255-136dup	ENSP00000439307.2:n.*1255-137_*1255-136dup
ENST00000546971.5:n.498-137_498-136dup
ENST00000548202.5:n.124_125dup
ENST00000548944.1:c.134-3881_134-3880dup	ENSP00000449071.1:n.134-3881_134-3880dup
ENST00000549048.1:n.419-137_419-136dup
ENST00000628866.2:c.*1255-137_*1255-136dup	ENSP00000486738.1:n.*1255-137_*1255-136dup
NM_004990.3:c.1754-137_1754-136dup	NP_004981.2:n.1754-137_1754-136dup
XM_006719398.2:c.1052-137_1052-136dup	XP_006719461.1:n.1052-137_1052-136dup
XM_011538353.1:c.*46-137_*46-136dup	XP_011536655.1:n.*46-137_*46-136dup
XM_006719398.4:c.1052-137_1052-136dup	XP_006719461.1:n.1052-137_1052-136dup
XR_001748704.2:n.1710-137_1710-136dup
XR_002957327.1:n.1701-137_1701-136dup
NM_004990.4:c.1754-137_1754-136dup MANE Select	NP_004981.2:n.1754-137_1754-136dup