Canonical Allele Identifier: CA2619465749

Gene: MARS1

Linked Data

• gnomAD v4: 12-57511943-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57511943A>G , CM000674.2:g.57511943A>G	GRCh38
NC_000012.11:g.57905726A>G , CM000674.1:g.57905726A>G	GRCh37
NC_000012.10:g.56191993A>G	NCBI36
NG_034077.1:g.28991A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1540-65A>G MANE Select	ENSP00000262027.5:n.1540-65A>G
ENST00000262027.9:c.1540-65A>G	ENSP00000262027.5:n.1540-65A>G
ENST00000447721.6:n.1182-65A>G
ENST00000537638.6:c.1540-65A>G	ENSP00000446168.2:n.1540-65A>G
ENST00000545888.6:c.*1041-65A>G	ENSP00000439307.2:n.*1041-65A>G
ENST00000546971.5:n.284-65A>G
ENST00000548630.1:n.101-65A>G
ENST00000548944.1:c.134-4552A>G	ENSP00000449071.1:n.134-4552A>G
ENST00000549048.1:n.73-65A>G
ENST00000628866.2:c.*1041-65A>G	ENSP00000486738.1:n.*1041-65A>G
NM_004990.3:c.1540-65A>G	NP_004981.2:n.1540-65A>G
XM_006719398.2:c.838-65A>G	XP_006719461.1:n.838-65A>G
XM_011538353.1:c.1540-65A>G	XP_011536655.1:n.1540-65A>G
XM_006719398.4:c.838-65A>G	XP_006719461.1:n.838-65A>G
XR_001748704.2:n.1563-65A>G
XR_002957327.1:n.1487-65A>G
NM_004990.4:c.1540-65A>G MANE Select	NP_004981.2:n.1540-65A>G