Canonical Allele Identifier: CA1672894393
Gene: ARMT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151468207A= , CM000668.2:g.151468207A= GRCh38
NC_000006.11:g.151789342A= , CM000668.1:g.151789342A= GRCh37
NC_000006.10:g.151831035A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367294.4:c.559-136A= MANE Select ENSP00000356263.3:n.559-136A=
ENST00000367294.3:c.559-136A= ENSP00000356263.3:n.559-136A=
ENST00000494826.1:c.*282-136A= ENSP00000435882.1:n.*282-136A=
ENST00000545879.5:c.202-136A= ENSP00000444121.1:n.202-136A=
NM_001286562.1:c.202-136A= NP_001273491.1:n.202-136A=
NM_024573.2:c.559-136A= NP_078849.1:n.559-136A=
NM_024573.3:c.559-136A= MANE Select NP_078849.1:n.559-136A=
NM_001286562.2:c.202-136A= NP_001273491.1:n.202-136A=
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