Canonical Allele Identifier: CA2534017497
Gene: ARMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151468188G>A , CM000668.2:g.151468188G>A GRCh38
NC_000006.11:g.151789323G>A , CM000668.1:g.151789323G>A GRCh37
NC_000006.10:g.151831016G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367294.4:c.559-155G>A MANE Select ENSP00000356263.3:n.559-155G>A
ENST00000367294.3:c.559-155G>A ENSP00000356263.3:n.559-155G>A
ENST00000494826.1:c.*282-155G>A ENSP00000435882.1:n.*282-155G>A
ENST00000545879.5:c.202-155G>A ENSP00000444121.1:n.202-155G>A
NM_001286562.1:c.202-155G>A NP_001273491.1:n.202-155G>A
NM_024573.2:c.559-155G>A NP_078849.1:n.559-155G>A
NM_024573.3:c.559-155G>A MANE Select NP_078849.1:n.559-155G>A
NM_001286562.2:c.202-155G>A NP_001273491.1:n.202-155G>A