Canonical Allele Identifier: CA1672894355
Gene: ARMT1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151468169A= , CM000668.2:g.151468169A= GRCh38
NC_000006.11:g.151789304A= , CM000668.1:g.151789304A= GRCh37
NC_000006.10:g.151830997A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367294.4:c.559-174A= MANE Select ENSP00000356263.3:n.559-174A=
ENST00000367294.3:c.559-174A= ENSP00000356263.3:n.559-174A=
ENST00000494826.1:c.*282-174A= ENSP00000435882.1:n.*282-174A=
ENST00000545879.5:c.202-174A= ENSP00000444121.1:n.202-174A=
NM_001286562.1:c.202-174A= NP_001273491.1:n.202-174A=
NM_024573.2:c.559-174A= NP_078849.1:n.559-174A=
NM_024573.3:c.559-174A= MANE Select NP_078849.1:n.559-174A=
NM_001286562.2:c.202-174A= NP_001273491.1:n.202-174A=
Search 100 bp 5'
Search 100 bp 3'