Canonical Allele Identifier: CA2619465986

Gene: MARS1

Linked Data

• gnomAD v4: 12-57512629-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57512629G>T , CM000674.2:g.57512629G>T	GRCh38
NC_000012.11:g.57906412G>T , CM000674.1:g.57906412G>T	GRCh37
NC_000012.10:g.56192679G>T	NCBI36
NG_034077.1:g.29677G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1754-122G>T MANE Select	ENSP00000262027.5:n.1754-122G>T
ENST00000262027.9:c.1754-122G>T	ENSP00000262027.5:n.1754-122G>T
ENST00000537638.6:c.*46-122G>T	ENSP00000446168.2:n.*46-122G>T
ENST00000545888.6:c.*1255-122G>T	ENSP00000439307.2:n.*1255-122G>T
ENST00000546971.5:n.498-122G>T
ENST00000548202.5:n.139G>T
ENST00000548944.1:c.134-3866G>T	ENSP00000449071.1:n.134-3866G>T
ENST00000549048.1:n.419-122G>T
ENST00000628866.2:c.*1255-122G>T	ENSP00000486738.1:n.*1255-122G>T
NM_004990.3:c.1754-122G>T	NP_004981.2:n.1754-122G>T
XM_006719398.2:c.1052-122G>T	XP_006719461.1:n.1052-122G>T
XM_011538353.1:c.*46-122G>T	XP_011536655.1:n.*46-122G>T
XM_006719398.4:c.1052-122G>T	XP_006719461.1:n.1052-122G>T
XR_001748704.2:n.1710-122G>T
XR_002957327.1:n.1701-122G>T
NM_004990.4:c.1754-122G>T MANE Select	NP_004981.2:n.1754-122G>T