Canonical Allele Identifier: CA1095890492
Gene: ARMT1 HGNC NCBI

Linked Data

dbSNP Id: rs528029911
gnomAD v3: 6-151468162-A-T
gnomAD v4: 6-151468162-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151468162A>T , CM000668.2:g.151468162A>T GRCh38
NC_000006.11:g.151789297A>T , CM000668.1:g.151789297A>T GRCh37
NC_000006.10:g.151830990A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367294.4:c.559-181A>T MANE Select ENSP00000356263.3:n.559-181A>T
ENST00000367294.3:c.559-181A>T ENSP00000356263.3:n.559-181A>T
ENST00000494826.1:c.*282-181A>T ENSP00000435882.1:n.*282-181A>T
ENST00000545879.5:c.202-181A>T ENSP00000444121.1:n.202-181A>T
NM_001286562.1:c.202-181A>T NP_001273491.1:n.202-181A>T
NM_024573.2:c.559-181A>T NP_078849.1:n.559-181A>T
NM_024573.3:c.559-181A>T MANE Select NP_078849.1:n.559-181A>T
NM_001286562.2:c.202-181A>T NP_001273491.1:n.202-181A>T
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