Canonical Allele Identifier: CA2038898282

Gene: MARS1

Linked Data

• dbSNP Id: rs965917822
• gnomAD v4: 12-57511583-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57511591_57511592dup , CM000674.2:g.57511591_57511592dup	GRCh38
NC_000012.11:g.57905374_57905375dup , CM000674.1:g.57905374_57905375dup	GRCh37
NC_000012.10:g.56191641_56191642dup	NCBI36
NG_034077.1:g.28639_28640dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1369-107_1369-106dup MANE Select	ENSP00000262027.5:n.1369-107_1369-106dup
ENST00000262027.9:c.1369-107_1369-106dup	ENSP00000262027.5:n.1369-107_1369-106dup
ENST00000447721.6:n.1011-107_1011-106dup
ENST00000537638.6:c.1369-107_1369-106dup	ENSP00000446168.2:n.1369-107_1369-106dup
ENST00000545888.6:c.*870-107_*870-106dup	ENSP00000439307.2:n.*870-107_*870-106dup
ENST00000548944.1:c.134-4904_134-4903dup	ENSP00000449071.1:n.134-4904_134-4903dup
ENST00000549603.1:n.315-107_315-106dup
ENST00000628866.2:c.*870-107_*870-106dup	ENSP00000486738.1:n.*870-107_*870-106dup
NM_004990.3:c.1369-107_1369-106dup	NP_004981.2:n.1369-107_1369-106dup
XM_006719398.2:c.667-107_667-106dup	XP_006719461.1:n.667-107_667-106dup
XM_011538353.1:c.1369-107_1369-106dup	XP_011536655.1:n.1369-107_1369-106dup
XM_006719398.4:c.667-107_667-106dup	XP_006719461.1:n.667-107_667-106dup
XR_001748704.2:n.1392-107_1392-106dup
XR_002957327.1:n.1316-107_1316-106dup
NM_004990.4:c.1369-107_1369-106dup MANE Select	NP_004981.2:n.1369-107_1369-106dup