Canonical Allele Identifier: CA2619465995

Gene: MARS1

Linked Data

• gnomAD v4: 12-57512640-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57512640C>A , CM000674.2:g.57512640C>A	GRCh38
NC_000012.11:g.57906423C>A , CM000674.1:g.57906423C>A	GRCh37
NC_000012.10:g.56192690C>A	NCBI36
NG_034077.1:g.29688C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1754-111C>A MANE Select	ENSP00000262027.5:n.1754-111C>A
ENST00000262027.9:c.1754-111C>A	ENSP00000262027.5:n.1754-111C>A
ENST00000537638.6:c.*46-111C>A	ENSP00000446168.2:n.*46-111C>A
ENST00000545888.6:c.*1255-111C>A	ENSP00000439307.2:n.*1255-111C>A
ENST00000546971.5:n.498-111C>A
ENST00000548202.5:n.150C>A
ENST00000548944.1:c.134-3855C>A	ENSP00000449071.1:n.134-3855C>A
ENST00000549048.1:n.419-111C>A
ENST00000628866.2:c.*1255-111C>A	ENSP00000486738.1:n.*1255-111C>A
NM_004990.3:c.1754-111C>A	NP_004981.2:n.1754-111C>A
XM_006719398.2:c.1052-111C>A	XP_006719461.1:n.1052-111C>A
XM_011538353.1:c.*46-111C>A	XP_011536655.1:n.*46-111C>A
XM_006719398.4:c.1052-111C>A	XP_006719461.1:n.1052-111C>A
XR_001748704.2:n.1710-111C>A
XR_002957327.1:n.1701-111C>A
NM_004990.4:c.1754-111C>A MANE Select	NP_004981.2:n.1754-111C>A