Canonical Allele Identifier: CA2038898231

Gene: MARS1

Linked Data

• dbSNP Id: rs1877511588
• gnomAD v4: 12-57511482-TAGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57511487_57511489del , CM000674.2:g.57511487_57511489del	GRCh38
NC_000012.11:g.57905270_57905272del , CM000674.1:g.57905270_57905272del	GRCh37
NC_000012.10:g.56191537_56191539del	NCBI36
NG_034077.1:g.28535_28537del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1369-211_1369-209del MANE Select	ENSP00000262027.5:n.1369-211_1369-209del
ENST00000262027.9:c.1369-211_1369-209del	ENSP00000262027.5:n.1369-211_1369-209del
ENST00000447721.6:n.1011-211_1011-209del
ENST00000537638.6:c.1369-211_1369-209del	ENSP00000446168.2:n.1369-211_1369-209del
ENST00000545888.6:c.*870-211_*870-209del	ENSP00000439307.2:n.*870-211_*870-209del
ENST00000548944.1:c.134-5008_134-5006del	ENSP00000449071.1:n.134-5008_134-5006del
ENST00000549603.1:n.315-211_315-209del
ENST00000628866.2:c.*870-211_*870-209del	ENSP00000486738.1:n.*870-211_*870-209del
NM_004990.3:c.1369-211_1369-209del	NP_004981.2:n.1369-211_1369-209del
XM_006719398.2:c.667-211_667-209del	XP_006719461.1:n.667-211_667-209del
XM_011538353.1:c.1369-211_1369-209del	XP_011536655.1:n.1369-211_1369-209del
XM_006719398.4:c.667-211_667-209del	XP_006719461.1:n.667-211_667-209del
XR_001748704.2:n.1392-211_1392-209del
XR_002957327.1:n.1316-211_1316-209del
NM_004990.4:c.1369-211_1369-209del MANE Select	NP_004981.2:n.1369-211_1369-209del