Canonical Allele Identifier: CA2578772426
Gene: ARMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151468265C>A , CM000668.2:g.151468265C>A GRCh38
NC_000006.11:g.151789400C>A , CM000668.1:g.151789400C>A GRCh37
NC_000006.10:g.151831093C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367294.4:c.559-78C>A MANE Select ENSP00000356263.3:n.559-78C>A
ENST00000367294.3:c.559-78C>A ENSP00000356263.3:n.559-78C>A
ENST00000494826.1:c.*282-78C>A ENSP00000435882.1:n.*282-78C>A
ENST00000545879.5:c.202-78C>A ENSP00000444121.1:n.202-78C>A
NM_001286562.1:c.202-78C>A NP_001273491.1:n.202-78C>A
NM_024573.2:c.559-78C>A NP_078849.1:n.559-78C>A
NM_024573.3:c.559-78C>A MANE Select NP_078849.1:n.559-78C>A
NM_001286562.2:c.202-78C>A NP_001273491.1:n.202-78C>A