Canonical Allele Identifier: CA2038898446

Gene: MARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57511906_57511907delinsTG , CM000674.2:g.57511906_57511907delinsTG	GRCh38
NC_000012.11:g.57905689_57905690delinsTG , CM000674.1:g.57905689_57905690delinsTG	GRCh37
NC_000012.10:g.56191956_56191957delinsTG	NCBI36
NG_034077.1:g.28954_28955delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1539+38_1539+39delinsTG MANE Select	ENSP00000262027.5:n.1539+38_1539+39delinsTG
ENST00000262027.9:c.1539+38_1539+39delinsTG	ENSP00000262027.5:n.1539+38_1539+39delinsTG
ENST00000447721.6:n.1181+38_1181+39delinsTG
ENST00000537638.6:c.1539+38_1539+39delinsTG	ENSP00000446168.2:n.1539+38_1539+39delinsTG
ENST00000545888.6:c.*1040+38_*1040+39delinsTG	ENSP00000439307.2:n.*1040+38_*1040+39delinsTG
ENST00000546971.5:n.283+38_283+39delinsTG
ENST00000548630.1:n.100+38_100+39delinsTG
ENST00000548944.1:c.134-4589_134-4588delinsTG	ENSP00000449071.1:n.134-4589_134-4588delinsTG
ENST00000549048.1:n.72+38_72+39delinsTG
ENST00000628866.2:c.*1040+38_*1040+39delinsTG	ENSP00000486738.1:n.*1040+38_*1040+39delinsTG
NM_004990.3:c.1539+38_1539+39delinsTG	NP_004981.2:n.1539+38_1539+39delinsTG
XM_006719398.2:c.837+38_837+39delinsTG	XP_006719461.1:n.837+38_837+39delinsTG
XM_011538353.1:c.1539+38_1539+39delinsTG	XP_011536655.1:n.1539+38_1539+39delinsTG
XM_006719398.4:c.837+38_837+39delinsTG	XP_006719461.1:n.837+38_837+39delinsTG
XR_001748704.2:n.1562+38_1562+39delinsTG
XR_002957327.1:n.1486+38_1486+39delinsTG
NM_004990.4:c.1539+38_1539+39delinsTG MANE Select	NP_004981.2:n.1539+38_1539+39delinsTG