Canonical Allele Identifier: CA1672894361

Gene: ARMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151468171_151468173delinsCAT , CM000668.2:g.151468171_151468173delinsCAT	GRCh38
NC_000006.11:g.151789306_151789308delinsCAT , CM000668.1:g.151789306_151789308delinsCAT	GRCh37
NC_000006.10:g.151830999_151831001delinsCAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367294.4:c.559-172_559-170delinsCAT MANE Select	ENSP00000356263.3:n.559-172_559-170delinsCAT
ENST00000367294.3:c.559-172_559-170delinsCAT	ENSP00000356263.3:n.559-172_559-170delinsCAT
ENST00000494826.1:c.*282-172_*282-170delinsCAT	ENSP00000435882.1:n.*282-172_*282-170delinsCAT
ENST00000545879.5:c.202-172_202-170delinsCAT	ENSP00000444121.1:n.202-172_202-170delinsCAT
NM_001286562.1:c.202-172_202-170delinsCAT	NP_001273491.1:n.202-172_202-170delinsCAT
NM_024573.2:c.559-172_559-170delinsCAT	NP_078849.1:n.559-172_559-170delinsCAT
NM_024573.3:c.559-172_559-170delinsCAT MANE Select	NP_078849.1:n.559-172_559-170delinsCAT
NM_001286562.2:c.202-172_202-170delinsCAT	NP_001273491.1:n.202-172_202-170delinsCAT