Canonical Allele Identifier: CA2038903299

Gene: MARS1 MIR6758

Linked Data

• ClinVar Variation Id: 1681754
• ClinVar RCV Id: RCV002239253
• dbSNP Id: rs1877582119
• gnomAD v4: 12-57512740-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57512740C>T , CM000674.2:g.57512740C>T	GRCh38
NC_000012.11:g.57906523C>T , CM000674.1:g.57906523C>T	GRCh37
NC_000012.10:g.56192790C>T	NCBI36
NG_034077.1:g.29788C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262027.10:c.1754-11C>T (MARS1) MANE Select	ENSP00000262027.5:n.1754-11C>T
ENST00000262027.9:c.1754-11C>T (MARS1)	ENSP00000262027.5:n.1754-11C>T
ENST00000537638.6:c.*46-11C>T (MARS1)	ENSP00000446168.2:n.*46-11C>T
ENST00000545888.6:c.*1255-11C>T (MARS1)	ENSP00000439307.2:n.*1255-11C>T
ENST00000546971.5:n.498-11C>T (MARS1)
ENST00000548202.5:n.250C>T (MARS1)
ENST00000548944.1:c.134-3755C>T (MARS1)	ENSP00000449071.1:n.134-3755C>T
ENST00000549048.1:n.419-11C>T (MARS1)
ENST00000628866.2:c.*1255-11C>T (MARS1)	ENSP00000486738.1:n.*1255-11C>T
NM_004990.3:c.1754-11C>T (MARS1)	NP_004981.2:n.1754-11C>T
NR_106816.1:n.53C>T (MIR6758)
XM_006719398.2:c.1052-11C>T (MARS1)	XP_006719461.1:n.1052-11C>T
XM_011538353.1:c.*46-11C>T (MARS1)	XP_011536655.1:n.*46-11C>T
XM_006719398.4:c.1052-11C>T (MARS1)	XP_006719461.1:n.1052-11C>T
XR_001748704.2:n.1710-11C>T (MARS1)
XR_002957327.1:n.1701-11C>T (MARS1)
NM_004990.4:c.1754-11C>T (MARS1) MANE Select	NP_004981.2:n.1754-11C>T