Canonical Allele Identifier: CA1672894328

Gene: ARMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151468155_151468158delinsCTTG , CM000668.2:g.151468155_151468158delinsCTTG	GRCh38
NC_000006.11:g.151789290_151789293delinsCTTG , CM000668.1:g.151789290_151789293delinsCTTG	GRCh37
NC_000006.10:g.151830983_151830986delinsCTTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367294.4:c.559-188_559-185delinsCTTG MANE Select	ENSP00000356263.3:n.559-188_559-185delinsCTTG
ENST00000367294.3:c.559-188_559-185delinsCTTG	ENSP00000356263.3:n.559-188_559-185delinsCTTG
ENST00000494826.1:c.*282-188_*282-185delinsCTTG	ENSP00000435882.1:n.*282-188_*282-185delinsCTTG
ENST00000545879.5:c.202-188_202-185delinsCTTG	ENSP00000444121.1:n.202-188_202-185delinsCTTG
NM_001286562.1:c.202-188_202-185delinsCTTG	NP_001273491.1:n.202-188_202-185delinsCTTG
NM_024573.2:c.559-188_559-185delinsCTTG	NP_078849.1:n.559-188_559-185delinsCTTG
NM_024573.3:c.559-188_559-185delinsCTTG MANE Select	NP_078849.1:n.559-188_559-185delinsCTTG
NM_001286562.2:c.202-188_202-185delinsCTTG	NP_001273491.1:n.202-188_202-185delinsCTTG