Canonical Allele Identifier: CA2680797812
Gene: ARMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151468205G>T , CM000668.2:g.151468205G>T GRCh38
NC_000006.11:g.151789340G>T , CM000668.1:g.151789340G>T GRCh37
NC_000006.10:g.151831033G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367294.4:c.559-138G>T MANE Select ENSP00000356263.3:n.559-138G>T
ENST00000367294.3:c.559-138G>T ENSP00000356263.3:n.559-138G>T
ENST00000494826.1:c.*282-138G>T ENSP00000435882.1:n.*282-138G>T
ENST00000545879.5:c.202-138G>T ENSP00000444121.1:n.202-138G>T
NM_001286562.1:c.202-138G>T NP_001273491.1:n.202-138G>T
NM_024573.2:c.559-138G>T NP_078849.1:n.559-138G>T
NM_024573.3:c.559-138G>T MANE Select NP_078849.1:n.559-138G>T
NM_001286562.2:c.202-138G>T NP_001273491.1:n.202-138G>T