Canonical Allele Identifier: CA1672894402

Gene: ARMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151468211_151468212delinsAT , CM000668.2:g.151468211_151468212delinsAT	GRCh38
NC_000006.11:g.151789346_151789347delinsAT , CM000668.1:g.151789346_151789347delinsAT	GRCh37
NC_000006.10:g.151831039_151831040delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367294.4:c.559-132_559-131delinsAT MANE Select	ENSP00000356263.3:n.559-132_559-131delinsAT
ENST00000367294.3:c.559-132_559-131delinsAT	ENSP00000356263.3:n.559-132_559-131delinsAT
ENST00000494826.1:c.*282-132_*282-131delinsAT	ENSP00000435882.1:n.*282-132_*282-131delinsAT
ENST00000545879.5:c.202-132_202-131delinsAT	ENSP00000444121.1:n.202-132_202-131delinsAT
NM_001286562.1:c.202-132_202-131delinsAT	NP_001273491.1:n.202-132_202-131delinsAT
NM_024573.2:c.559-132_559-131delinsAT	NP_078849.1:n.559-132_559-131delinsAT
NM_024573.3:c.559-132_559-131delinsAT MANE Select	NP_078849.1:n.559-132_559-131delinsAT
NM_001286562.2:c.202-132_202-131delinsAT	NP_001273491.1:n.202-132_202-131delinsAT