Canonical Allele Identifier: CA2741258466

Gene: MARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57511881_57511882insCCACG , CM000674.2:g.57511881_57511882insCCACG	GRCh38
NC_000012.11:g.57905664_57905665insCCACG , CM000674.1:g.57905664_57905665insCCACG	GRCh37
NC_000012.10:g.56191931_56191932insCCACG	NCBI36
NG_034077.1:g.28929_28930insCCACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262027.10:c.1539+13_1539+14insCCACG MANE Select	ENSP00000262027.5:n.1539+13_1539+14insCCACG
ENST00000262027.9:c.1539+13_1539+14insCCACG	ENSP00000262027.5:n.1539+13_1539+14insCCACG
ENST00000447721.6:n.1181+13_1181+14insCCACG
ENST00000537638.6:c.1539+13_1539+14insCCACG	ENSP00000446168.2:n.1539+13_1539+14insCCACG
ENST00000545888.6:c.*1040+13_*1040+14insCCACG	ENSP00000439307.2:n.*1040+13_*1040+14insCCACG
ENST00000546971.5:n.283+13_283+14insCCACG
ENST00000548630.1:n.100+13_100+14insCCACG
ENST00000548944.1:c.134-4614_134-4613insCCACG	ENSP00000449071.1:n.134-4614_134-4613insCCACG
ENST00000549048.1:n.72+13_72+14insCCACG
ENST00000628866.2:c.*1040+13_*1040+14insCCACG	ENSP00000486738.1:n.*1040+13_*1040+14insCCACG
NM_004990.3:c.1539+13_1539+14insCCACG	NP_004981.2:n.1539+13_1539+14insCCACG
XM_006719398.2:c.837+13_837+14insCCACG	XP_006719461.1:n.837+13_837+14insCCACG
XM_011538353.1:c.1539+13_1539+14insCCACG	XP_011536655.1:n.1539+13_1539+14insCCACG
XM_006719398.4:c.837+13_837+14insCCACG	XP_006719461.1:n.837+13_837+14insCCACG
XR_001748704.2:n.1562+13_1562+14insCCACG
XR_002957327.1:n.1486+13_1486+14insCCACG
NM_004990.4:c.1539+13_1539+14insCCACG MANE Select	NP_004981.2:n.1539+13_1539+14insCCACG