Canonical Allele Identifier: CA1672894338
Gene: ARMT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151468158G= , CM000668.2:g.151468158G= GRCh38
NC_000006.11:g.151789293G= , CM000668.1:g.151789293G= GRCh37
NC_000006.10:g.151830986G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367294.4:c.559-185G= MANE Select ENSP00000356263.3:n.559-185G=
ENST00000367294.3:c.559-185G= ENSP00000356263.3:n.559-185G=
ENST00000494826.1:c.*282-185G= ENSP00000435882.1:n.*282-185G=
ENST00000545879.5:c.202-185G= ENSP00000444121.1:n.202-185G=
NM_001286562.1:c.202-185G= NP_001273491.1:n.202-185G=
NM_024573.2:c.559-185G= NP_078849.1:n.559-185G=
NM_024573.3:c.559-185G= MANE Select NP_078849.1:n.559-185G=
NM_001286562.2:c.202-185G= NP_001273491.1:n.202-185G=
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