Canonical Allele Identifier: CA1672894468
Gene: ARMT1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151468273C= , CM000668.2:g.151468273C= GRCh38
NC_000006.11:g.151789408C= , CM000668.1:g.151789408C= GRCh37
NC_000006.10:g.151831101C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367294.4:c.559-70C= MANE Select ENSP00000356263.3:n.559-70C=
ENST00000367294.3:c.559-70C= ENSP00000356263.3:n.559-70C=
ENST00000494826.1:c.*282-70C= ENSP00000435882.1:n.*282-70C=
ENST00000545879.5:c.202-70C= ENSP00000444121.1:n.202-70C=
NM_001286562.1:c.202-70C= NP_001273491.1:n.202-70C=
NM_024573.2:c.559-70C= NP_078849.1:n.559-70C=
NM_024573.3:c.559-70C= MANE Select NP_078849.1:n.559-70C=
NM_001286562.2:c.202-70C= NP_001273491.1:n.202-70C=
Search 100 bp 5'
Search 100 bp 3'