Canonical Allele Identifier: CA1672894330
Gene: ARMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151468155C= , CM000668.2:g.151468155C= GRCh38
NC_000006.11:g.151789290C= , CM000668.1:g.151789290C= GRCh37
NC_000006.10:g.151830983C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367294.4:c.559-188C= MANE Select ENSP00000356263.3:n.559-188C=
ENST00000367294.3:c.559-188C= ENSP00000356263.3:n.559-188C=
ENST00000494826.1:c.*282-188C= ENSP00000435882.1:n.*282-188C=
ENST00000545879.5:c.202-188C= ENSP00000444121.1:n.202-188C=
NM_001286562.1:c.202-188C= NP_001273491.1:n.202-188C=
NM_024573.2:c.559-188C= NP_078849.1:n.559-188C=
NM_024573.3:c.559-188C= MANE Select NP_078849.1:n.559-188C=
NM_001286562.2:c.202-188C= NP_001273491.1:n.202-188C=