Canonical Allele Identifier: CA2619465611

Gene: MARS1

Linked Data

• gnomAD v4: 12-57511619-AAAAGGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57511620_57511625del , CM000674.2:g.57511620_57511625del	GRCh38
NC_000012.11:g.57905403_57905408del , CM000674.1:g.57905403_57905408del	GRCh37
NC_000012.10:g.56191670_56191675del	NCBI36
NG_034077.1:g.28668_28673del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1369-78_1369-73del MANE Select	ENSP00000262027.5:n.1369-78_1369-73del
ENST00000262027.9:c.1369-78_1369-73del	ENSP00000262027.5:n.1369-78_1369-73del
ENST00000447721.6:n.1011-78_1011-73del
ENST00000537638.6:c.1369-78_1369-73del	ENSP00000446168.2:n.1369-78_1369-73del
ENST00000545888.6:c.*870-78_*870-73del	ENSP00000439307.2:n.*870-78_*870-73del
ENST00000546971.5:n.35_40del
ENST00000548944.1:c.134-4875_134-4870del	ENSP00000449071.1:n.134-4875_134-4870del
ENST00000549603.1:n.315-78_315-73del
ENST00000628866.2:c.*870-78_*870-73del	ENSP00000486738.1:n.*870-78_*870-73del
NM_004990.3:c.1369-78_1369-73del	NP_004981.2:n.1369-78_1369-73del
XM_006719398.2:c.667-78_667-73del	XP_006719461.1:n.667-78_667-73del
XM_011538353.1:c.1369-78_1369-73del	XP_011536655.1:n.1369-78_1369-73del
XM_006719398.4:c.667-78_667-73del	XP_006719461.1:n.667-78_667-73del
XR_001748704.2:n.1392-78_1392-73del
XR_002957327.1:n.1316-78_1316-73del
NM_004990.4:c.1369-78_1369-73del MANE Select	NP_004981.2:n.1369-78_1369-73del