Canonical Allele Identifier: CA1672894362

Gene: ARMT1

Linked Data

• dbSNP Id: rs1781548230

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151468172_151468173del , CM000668.2:g.151468172_151468173del	GRCh38
NC_000006.11:g.151789307_151789308del , CM000668.1:g.151789307_151789308del	GRCh37
NC_000006.10:g.151831000_151831001del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367294.4:c.559-171_559-170del MANE Select	ENSP00000356263.3:n.559-171_559-170del
ENST00000367294.3:c.559-171_559-170del	ENSP00000356263.3:n.559-171_559-170del
ENST00000494826.1:c.*282-171_*282-170del	ENSP00000435882.1:n.*282-171_*282-170del
ENST00000545879.5:c.202-171_202-170del	ENSP00000444121.1:n.202-171_202-170del
NM_001286562.1:c.202-171_202-170del	NP_001273491.1:n.202-171_202-170del
NM_024573.2:c.559-171_559-170del	NP_078849.1:n.559-171_559-170del
NM_024573.3:c.559-171_559-170del MANE Select	NP_078849.1:n.559-171_559-170del
NM_001286562.2:c.202-171_202-170del	NP_001273491.1:n.202-171_202-170del