Canonical Allele Identifier: CA2619465617

Gene: MARS1

Linked Data

• gnomAD v4: 12-57511627-ATATGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57511628_57511632del , CM000674.2:g.57511628_57511632del	GRCh38
NC_000012.11:g.57905411_57905415del , CM000674.1:g.57905411_57905415del	GRCh37
NC_000012.10:g.56191678_56191682del	NCBI36
NG_034077.1:g.28676_28680del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1369-70_1369-66del MANE Select	ENSP00000262027.5:n.1369-70_1369-66del
ENST00000262027.9:c.1369-70_1369-66del	ENSP00000262027.5:n.1369-70_1369-66del
ENST00000447721.6:n.1011-70_1011-66del
ENST00000537638.6:c.1369-70_1369-66del	ENSP00000446168.2:n.1369-70_1369-66del
ENST00000545888.6:c.*870-70_*870-66del	ENSP00000439307.2:n.*870-70_*870-66del
ENST00000546971.5:n.43_47del
ENST00000548944.1:c.134-4867_134-4863del	ENSP00000449071.1:n.134-4867_134-4863del
ENST00000549603.1:n.315-70_315-66del
ENST00000628866.2:c.*870-70_*870-66del	ENSP00000486738.1:n.*870-70_*870-66del
NM_004990.3:c.1369-70_1369-66del	NP_004981.2:n.1369-70_1369-66del
XM_006719398.2:c.667-70_667-66del	XP_006719461.1:n.667-70_667-66del
XM_011538353.1:c.1369-70_1369-66del	XP_011536655.1:n.1369-70_1369-66del
XM_006719398.4:c.667-70_667-66del	XP_006719461.1:n.667-70_667-66del
XR_001748704.2:n.1392-70_1392-66del
XR_002957327.1:n.1316-70_1316-66del
NM_004990.4:c.1369-70_1369-66del MANE Select	NP_004981.2:n.1369-70_1369-66del